RESTful Lookup — Test-Drive (2007 – 2026)

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{
  "NDC": [
    {
      "NDCCode": "50114-7026-1",
      "PackageDescription": "10 AMPULE in 1 CARTON (50114-7026-1)  > 1.1 mL in 1 AMPULE",
      "NDC11Code": "50114-7026-01",
      "ProductNDC": "50114-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Lymphomyosot",
      "NonProprietaryName": "Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
      "StartMarketingDate": "20100401",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "ARANEUS DIADEMATUS; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; LEVOTHYROXINE; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SMILAX REGELII ROOT; SODIUM SULFATE; TEUCRIUM SCORODONIA FLOWERING TOP; TRIBASIC CALCIUM PHOSPHATE; VERONICA OFFICINALIS FLOWERING TOP",
      "StrengthNumber": "6; 4; 12; 4; 5; 4; 3; 3; 12; 3; 4; 4; 3; 6; 4; 3; 12; 3",
      "StrengthUnit": "[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL",
      "Pharm_Classes": "l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]",
      "Status": "Deprecated",
      "LastUpdate": "2015-01-16"
    },
    {
      "NDCCode": "50114-7026-2",
      "PackageDescription": "1 AMPULE in 1 CARTON (50114-7026-2)  > 1.1 mL in 1 AMPULE",
      "NDC11Code": "50114-7026-02",
      "ProductNDC": "50114-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Lymphomyosot",
      "NonProprietaryName": "Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
      "StartMarketingDate": "20100401",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "ARANEUS DIADEMATUS; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; LEVOTHYROXINE; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SMILAX REGELII ROOT; SODIUM SULFATE; TEUCRIUM SCORODONIA FLOWERING TOP; TRIBASIC CALCIUM PHOSPHATE; VERONICA OFFICINALIS FLOWERING TOP",
      "StrengthNumber": "6; 4; 12; 4; 5; 4; 3; 3; 12; 3; 4; 4; 3; 6; 4; 3; 12; 3",
      "StrengthUnit": "[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL",
      "Pharm_Classes": "l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]",
      "Status": "Deprecated",
      "LastUpdate": "2015-01-16"
    },
    {
      "NDCCode": "0002-7026-60",
      "PackageDescription": "60 TABLET, COATED in 1 BOTTLE (0002-7026-60) ",
      "NDC11Code": "00002-7026-60",
      "ProductNDC": "0002-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Jaypirca",
      "NonProprietaryName": "Pirtobrutinib",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20230127",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA216059",
      "LabelerName": "Eli Lilly and Company",
      "SubstanceName": "PIRTOBRUTINIB",
      "StrengthNumber": "100",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Breast Cancer Resistance Protein Inhibitors [MoA], Bruton's Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-03-24",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20230127",
      "SamplePackage": "N",
      "IndicationAndUsage": "JAYPIRCA® is a kinase inhibitor indicated for the treatment of: : 1 Adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two lines of systemic therapy, including a BTK inhibitor. (1.1).This indication is approved under accelerated approval based on response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. , 2 Adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent BTK inhibitor. (1.2).",
      "Description": "Pirtobrutinib is a kinase inhibitor. It is an orally available, small molecule ATP-competitive inhibitor of BTK. The active pharmaceutical ingredient is pirtobrutinib with the molecular formula C22H21F4N5O3 and a molecular weight of 479.44 g/mol. The chemical name for pirtobrutinib is 5-amino-3-{4-[(5-fluoro-2-methoxybenzamido)methyl]phenyl}-1-[(2S)-1,1,1-trifluoropropan-2-yl]-1H-pyrazole-4-carboxamide. Pirtobrutinib is a white to practically white to yellow to brown solid. The aqueous solubility of pirtobrutinib is considered practically insoluble, or insoluble, across the pH 1 to pH 7 range. Pirtobrutinib tablets are supplied as 50 mg or 100 mg film-coated, debossed tablets for oral administration. Each tablet contains inactive ingredients of croscarmellose sodium, hypromellose acetate succinate, lactose monohydrate, magnesium stearate, microcrystalline cellulose and silicon dioxide. The tablet film coating material contains FD&C Blue #2, hypromellose, titanium dioxide and triacetin."
    },
    {
      "NDCCode": "0002-7026-99",
      "PackageDescription": "30 TABLET, COATED in 1 BOTTLE (0002-7026-99) ",
      "NDC11Code": "00002-7026-99",
      "ProductNDC": "0002-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Jaypirca",
      "NonProprietaryName": "Pirtobrutinib",
      "DosageFormName": "TABLET, COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20230127",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA216059",
      "LabelerName": "Eli Lilly and Company",
      "SubstanceName": "PIRTOBRUTINIB",
      "StrengthNumber": "100",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Breast Cancer Resistance Protein Inhibitors [MoA], Bruton's Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA]",
      "Status": "Active",
      "LastUpdate": "2026-03-24",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20230215",
      "SamplePackage": "Y",
      "IndicationAndUsage": "JAYPIRCA® is a kinase inhibitor indicated for the treatment of: : 1 Adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two lines of systemic therapy, including a BTK inhibitor. (1.1).This indication is approved under accelerated approval based on response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. , 2 Adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent BTK inhibitor. (1.2).",
      "Description": "Pirtobrutinib is a kinase inhibitor. It is an orally available, small molecule ATP-competitive inhibitor of BTK. The active pharmaceutical ingredient is pirtobrutinib with the molecular formula C22H21F4N5O3 and a molecular weight of 479.44 g/mol. The chemical name for pirtobrutinib is 5-amino-3-{4-[(5-fluoro-2-methoxybenzamido)methyl]phenyl}-1-[(2S)-1,1,1-trifluoropropan-2-yl]-1H-pyrazole-4-carboxamide. Pirtobrutinib is a white to practically white to yellow to brown solid. The aqueous solubility of pirtobrutinib is considered practically insoluble, or insoluble, across the pH 1 to pH 7 range. Pirtobrutinib tablets are supplied as 50 mg or 100 mg film-coated, debossed tablets for oral administration. Each tablet contains inactive ingredients of croscarmellose sodium, hypromellose acetate succinate, lactose monohydrate, magnesium stearate, microcrystalline cellulose and silicon dioxide. The tablet film coating material contains FD&C Blue #2, hypromellose, titanium dioxide and triacetin."
    },
    {
      "NDCCode": "0338-7026-06",
      "PackageDescription": "6 BAG in 1 CARTON (0338-7026-06)  / 1000 mL in 1 BAG (0338-7026-01) ",
      "NDC11Code": "00338-7026-06",
      "ProductNDC": "0338-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Clinimix E",
      "NonProprietaryName": "Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20240715",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA020678",
      "LabelerName": "Baxter Healthcare Company",
      "SubstanceName": "LEUCINE; PHENYLALANINE; LYSINE; METHIONINE; ISOLEUCINE; VALINE; HISTIDINE; THREONINE; TRYPTOPHAN; ALANINE; GLYCINE; ARGININE; PROLINE; SERINE; TYROSINE; SODIUM ACETATE; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; CALCIUM CHLORIDE; DEXTROSE",
      "StrengthNumber": "311; 238; 247; 170; 255; 247; 204; 179; 77; 880; 438; 489; 289; 213; 17; 297; 261; 51; 77; 33; 10",
      "StrengthUnit": "mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; g/100mL",
      "Pharm_Classes": "Amino Acid [EPC], Amino Acids [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
      "Status": "Active",
      "LastUpdate": "2026-06-06",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20240715",
      "SamplePackage": "N",
      "IndicationAndUsage": "CLINIMIX E is indicated as a source of calories, protein, and electrolytes for patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. CLINIMIX E may be used to treat negative nitrogen balance in patients.",
      "Description": "CLINIMIX E sulfite-free (amino acids with electrolytes in dextrose with calcium) injection for intravenous use consists of sterile, nonpyrogenic, hypertonic solutions in a dual chamber container. The outlet port chamber contains essential and nonessential amino acids with electrolytes. The formulas for the individual electrolytes and amino acids are provided in Table 8. The injection port chamber contains dextrose with calcium. The formula for Calcium Chloride is: CaCl22H2O. Dextrose, USP, is chemically designated D-glucose, monohydrate (C6H12O6  H2O) and has the following structure. Dextrose is derived from corn. See Table 7 for composition, pH, osmolarity, ionic concentration and caloric content of the admixed product [see Dosage Forms and Strengths (3)]. The dual chamber container is a lipid-compatible plastic container (PL 2401 Plastic). CLINIMIX E contains no more than 25 mcg/L of aluminum."
    },
    {
      "NDCCode": "0440-7026-30",
      "PackageDescription": "30 TABLET in 1 BOTTLE, PLASTIC (0440-7026-30)",
      "NDC11Code": "00440-7026-30",
      "ProductNDC": "0440-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Acetaminophen And Codeine",
      "NonProprietaryName": "Acetaminophen And Codeine Phosphate",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "19880930",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA089805",
      "LabelerName": "Liberty Pharmaceuticals, Inc.",
      "SubstanceName": "CODEINE PHOSPHATE; ACETAMINOPHEN",
      "StrengthNumber": "30; 300",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Full Opioid Agonists [MoA],Opioid Agonist [EPC]",
      "DEASchedule": "CIII",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231",
      "IndicationAndUsage": "Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain.",
      "Description": "Acetaminophen and codeine is supplied in tablet form for oral administration. Acetaminophen, 4'-hydroxyacetanilide, a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. It has the following structural formula. Codeine phosphate, 7,8-didehydro-4,5α-epoxy-3-methoxy-17methylmorphinan-6α-ol phosphate (1:1) (salt) hemihydrate, a white crystalline powder, is a narcotic analgesic and antitussive. It has the following structural formula. Each 300 mg/30 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................30 mg. Each 300 mg/60 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................60 mg."
    },
    {
      "NDCCode": "0440-7026-40",
      "PackageDescription": "40 TABLET in 1 BOTTLE, PLASTIC (0440-7026-40)",
      "NDC11Code": "00440-7026-40",
      "ProductNDC": "0440-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Acetaminophen And Codeine",
      "NonProprietaryName": "Acetaminophen And Codeine Phosphate",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "19880930",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA089805",
      "LabelerName": "Liberty Pharmaceuticals, Inc.",
      "SubstanceName": "CODEINE PHOSPHATE; ACETAMINOPHEN",
      "StrengthNumber": "30; 300",
      "StrengthUnit": "mg/1; mg/1",
      "Pharm_Classes": "Full Opioid Agonists [MoA],Opioid Agonist [EPC]",
      "DEASchedule": "CIII",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231",
      "IndicationAndUsage": "Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain.",
      "Description": "Acetaminophen and codeine is supplied in tablet form for oral administration. Acetaminophen, 4'-hydroxyacetanilide, a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. It has the following structural formula. Codeine phosphate, 7,8-didehydro-4,5α-epoxy-3-methoxy-17methylmorphinan-6α-ol phosphate (1:1) (salt) hemihydrate, a white crystalline powder, is a narcotic analgesic and antitussive. It has the following structural formula. Each 300 mg/30 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................30 mg. Each 300 mg/60 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................60 mg."
    },
    {
      "NDCCode": "0904-7026-61",
      "PackageDescription": "100 BLISTER PACK in 1 CARTON (0904-7026-61)  / 1 CAPSULE in 1 BLISTER PACK",
      "NDC11Code": "00904-7026-61",
      "ProductNDC": "0904-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Nitrofurantoin Macrocrystals",
      "NonProprietaryName": "Nitrofurantoin Macrocrystals",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20180215",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA205005",
      "LabelerName": "Major Pharmaceuticals",
      "SubstanceName": "NITROFURANTOIN",
      "StrengthNumber": "50",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Nitrofuran Antibacterial [EPC], Nitrofurans [CS]",
      "Status": "Active",
      "LastUpdate": "2026-03-24",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20180215",
      "SamplePackage": "N",
      "IndicationAndUsage": "Nitrofurantoin macrocrystals capsules are specifically indicated for the treatment of urinary tract infections when due to susceptible strains of Escherichia coli, enterococci, Staphylococcus aureus, and certain susceptible strains of Klebsiella and Enterobacter species. Nitrofurantoin is not indicated for the treatment of pyelonephritis or perinephric abscesses. To reduce the development of drug-resistant bacteria and maintain the effectiveness of nitrofurantoin macrocrystals capsules and other antibacterial drugs, nitrofurantoin macrocrystals capsules should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Nitrofurantoins lack the broader tissue distribution of other therapeutic agents approved for urinary tract infections. Consequently, many patients who are treated with nitrofurantoin macrocrystals capsules are predisposed to persistence or reappearance of bacteriuria. Urine specimens for culture and susceptibility testing should be obtained before and after completion of therapy. If persistence or reappearance of bacteriuria occurs after treatment with nitrofurantoin macrocrystals capsules, other therapeutic agents with broader tissue distribution should be selected. In considering the use of nitrofurantoin macrocrystals capsules, lower eradication rates should be balanced against the increased potential for systemic toxicity and for the development of antimicrobial resistance when agents with broader tissue distribution are utilized.",
      "Description": "Nitrofurantoin capsules, USP (macrocrystals) is a synthetic chemical of controlled crystal size. It is a stable, lemon-yellow, crystalline compound. Nitrofurantoin capsules, USP (macrocrystals) is an antibacterial agent for specific urinary tract infections. It is available in 50 mg and 100 mg capsules for oral administration. 1-[[(5-nitro-2-furanyl)methylene] amino]-2,4-imidazolidinedione. Nitrofurantoin macrocrystals is a lemon-yellow crystalline compound. It is soluble in dimethylformamide, very slightly soluble in water and in alcohol. Each nitrofurantoin capsules, USP (macrocrystals) intended for oral administration contains 50 mg and 100 mg of nitrofurantoin macrocrystals. In addition, each capsule contains the following inactive ingredients: gelatin, lactose monohydrate, magnesium stearate, pregelatinized starch, talc and titanium dioxide. Additionally each 50 mg and 100 mg capsule shell contains FD & C Blue # 1, FD & C Red # 3 and sodium lauryl sulphate. The capsule is printed with black pharmaceutical ink which contains black iron oxide, potassium hydroxide, propylene glycol and shellac."
    },
    {
      "NDCCode": "10888-7026-1",
      "PackageDescription": "18000 CAPSULE, LIQUID FILLED in 1 CARTON (10888-7026-1)",
      "NDC11Code": "10888-7026-01",
      "ProductNDC": "10888-7026",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Docusate Sodium",
      "DosageFormName": "CAPSULE, LIQUID FILLED",
      "StartMarketingDate": "20110701",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Banner Pharmacaps Inc",
      "SubstanceName": "DOCUSATE SODIUM",
      "StrengthNumber": "100",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "50090-7026-1",
      "PackageDescription": "12 CAPSULE in 1 BOTTLE (50090-7026-1) ",
      "NDC11Code": "50090-7026-01",
      "ProductNDC": "50090-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Cephalexin",
      "NonProprietaryName": "Cephalexin",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151019",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA090836",
      "LabelerName": "A-S Medication Solutions",
      "SubstanceName": "CEPHALEXIN",
      "StrengthNumber": "500",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Cephalosporin Antibacterial [EPC], Cephalosporins [CS]",
      "Status": "Active",
      "LastUpdate": "2024-07-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20240108",
      "SamplePackage": "N",
      "IndicationAndUsage": "Cephalexin is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria: 1 Respiratory tract infection (1.1), 2 Otitis media (1.2), 3 Skin and skin structure infections (1.3), 4 Bone infections (1.4), 5 Genitourinary tract infections (1.5).",
      "Description": "Cephalexin capsules, USP is a semisynthetic cephalosporin antibacterial drug intended for oral administration. It is 7-(D-α-Amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate. Cephalexin has the molecular formula C 16H 17N 3O 4SH 2O and the molecular weight is 365.41. Cephalexin has the following structural formula. Each capsule contains cephalexin monohydrate equivalent to 250 mg, 333 mg, 500 mg, or 750 mg of cephalexin. The 250 mg, 333 mg, 500 mg and 750 mg capsules contain anhydrous lactose, colloidal silicon dioxide, magnesium stearate, FD & C Blue No. 1, D & C Yellow No. 10, gelatin, sodium lauryl sulphate, titanium dioxide. In addition, the 250 mg capsule contains FD & C Red No. 40; 333 mg and 750 mg Capsules contains FD & C Yellow No. 6. The imprinting ink contains; shellac, propylene glycol, strong ammonia solution and potassium hydroxide. Also black Iron oxide is used in 250 mg, 333 mg and 500 mg and titanium dioxide is used in 750 mg."
    },
    {
      "NDCCode": "50090-7026-3",
      "PackageDescription": "6 CAPSULE in 1 BOTTLE (50090-7026-3) ",
      "NDC11Code": "50090-7026-03",
      "ProductNDC": "50090-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Cephalexin",
      "NonProprietaryName": "Cephalexin",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20151019",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA090836",
      "LabelerName": "A-S Medication Solutions",
      "SubstanceName": "CEPHALEXIN",
      "StrengthNumber": "500",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Cephalosporin Antibacterial [EPC], Cephalosporins [CS]",
      "Status": "Active",
      "LastUpdate": "2024-07-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20240108",
      "SamplePackage": "N",
      "IndicationAndUsage": "Cephalexin is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria: 1 Respiratory tract infection (1.1), 2 Otitis media (1.2), 3 Skin and skin structure infections (1.3), 4 Bone infections (1.4), 5 Genitourinary tract infections (1.5).",
      "Description": "Cephalexin capsules, USP is a semisynthetic cephalosporin antibacterial drug intended for oral administration. It is 7-(D-α-Amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate. Cephalexin has the molecular formula C 16H 17N 3O 4SH 2O and the molecular weight is 365.41. Cephalexin has the following structural formula. Each capsule contains cephalexin monohydrate equivalent to 250 mg, 333 mg, 500 mg, or 750 mg of cephalexin. The 250 mg, 333 mg, 500 mg and 750 mg capsules contain anhydrous lactose, colloidal silicon dioxide, magnesium stearate, FD & C Blue No. 1, D & C Yellow No. 10, gelatin, sodium lauryl sulphate, titanium dioxide. In addition, the 250 mg capsule contains FD & C Red No. 40; 333 mg and 750 mg Capsules contains FD & C Yellow No. 6. The imprinting ink contains; shellac, propylene glycol, strong ammonia solution and potassium hydroxide. Also black Iron oxide is used in 250 mg, 333 mg and 500 mg and titanium dioxide is used in 750 mg."
    },
    {
      "NDCCode": "52731-7026-2",
      "PackageDescription": "1 BOTTLE in 1 BOX (52731-7026-2)  > 50 mL in 1 BOTTLE (52731-7026-1)",
      "NDC11Code": "52731-7026-02",
      "ProductNDC": "52731-7026",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Air Pollution Complex",
      "NonProprietaryName": "Arnica Montana 6x, Bovista 6x, Calcarea Carbonica 8x,carbo Vegetabilis 8x, Cicuta Virosa 6x, Euphorbium Officinarum 6x,hydrastis Canadensis 4x, Petroleum 6x, Phosphorus 8x, Plumbum Metallicum 8x, Sulf",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "20110601",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Nova Homeopathic Therapeutics, Inc.",
      "SubstanceName": "ARNICA MONTANA; GIANT PUFFBALL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; CICUTA VIROSA ROOT; EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; LIQUID PETROLEUM; PHOSPHORUS; LEAD; SULFUR",
      "StrengthNumber": "6; 6; 8; 8; 6; 6; 4; 6; 8; 8; 30",
      "StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "For oral use only."
    },
    {
      "NDCCode": "62670-7026-0",
      "PackageDescription": "29 mL in 1 BOTTLE (62670-7026-0) ",
      "NDC11Code": "62670-7026-00",
      "ProductNDC": "62670-7026",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Anti Bacterial Hand Gel",
      "ProprietaryNameSuffix": "Waikiki Beach Coconut",
      "NonProprietaryName": "Alcohol",
      "DosageFormName": "GEL",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20260209",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "505G(a)(3)",
      "LabelerName": "Bath & Body Works, Inc.",
      "SubstanceName": "ALCOHOL",
      "StrengthNumber": "71",
      "StrengthUnit": "mL/100mL",
      "Status": "Active",
      "LastUpdate": "2026-07-03",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20271231",
      "StartMarketingDatePackage": "20260209",
      "SamplePackage": "N",
      "IndicationAndUsage": "Decreases bacteria on hands."
    },
    {
      "NDCCode": "68788-7026-3",
      "PackageDescription": "30 TABLET in 1 BOTTLE (68788-7026-3) ",
      "NDC11Code": "68788-7026-03",
      "ProductNDC": "68788-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Levothyroxine Sodium",
      "NonProprietaryName": "Levothyroxine Sodium",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20171012",
      "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
      "ApplicationNumber": "NDA021342",
      "LabelerName": "Preferrred Pharmaeuticals Inc.",
      "SubstanceName": "LEVOTHYROXINE SODIUM",
      "StrengthNumber": "137",
      "StrengthUnit": "ug/1",
      "Pharm_Classes": "l-Thyroxine [EPC],Thyroxine [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2021-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20171012",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "68788-7026-9",
      "PackageDescription": "90 TABLET in 1 BOTTLE (68788-7026-9) ",
      "NDC11Code": "68788-7026-09",
      "ProductNDC": "68788-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Levothyroxine Sodium",
      "NonProprietaryName": "Levothyroxine Sodium",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20171012",
      "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
      "ApplicationNumber": "NDA021342",
      "LabelerName": "Preferrred Pharmaeuticals Inc.",
      "SubstanceName": "LEVOTHYROXINE SODIUM",
      "StrengthNumber": "137",
      "StrengthUnit": "ug/1",
      "Pharm_Classes": "l-Thyroxine [EPC],Thyroxine [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2021-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20201231",
      "StartMarketingDatePackage": "20171012",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "71872-7026-1",
      "PackageDescription": "1 VIAL, MULTI-DOSE in 1 BAG (71872-7026-1)  > 10 mL in 1 VIAL, MULTI-DOSE",
      "NDC11Code": "71872-7026-01",
      "ProductNDC": "71872-7026",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Quelicin",
      "NonProprietaryName": "Succinylcholine Chloride",
      "DosageFormName": "INJECTION, SOLUTION",
      "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
      "StartMarketingDate": "20140331",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA008845",
      "LabelerName": "Medical Purchasing Solutions, LLC",
      "SubstanceName": "SUCCINYLCHOLINE CHLORIDE",
      "StrengthNumber": "20",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2025-01-01",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "20180228",
      "SamplePackage": "N",
      "IndicationAndUsage": "Succinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.",
      "Description": "Quelicin (Succinylcholine Chloride Injection, USP) is a sterile, nonpyrogenic solution to be used as a short-acting, depolarizing, skeletal muscle relaxant. See HOW SUPPLIED for summary of content and characteristics of the solutions. The solutions are for I.M. or I.V. use. Succinylcholine Chloride, USP is chemically designated C 14H 30Cl 2N 2O 4 and its molecular weight is 361.31. It has the following structural formula. Succinylcholine is a diquaternary base consisting of the dichloride salt of the dicholine ester of succinic acid. It is a white, odorless, slightly bitter powder, very soluble in water. The drug is incompatible with alkaline solutions but relatively stable in acid solutions. Solutions of the drug lose potency unless refrigerated. Solution intended for multiple-dose administration contains 0.18% methylparaben and 0.02% propylparaben as preservatives (List No. 6629). Product not requiring dilution (multiple-dose fliptop vial) contains sodium chloride to render isotonic. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. pH is 3.6 (3.0 to 4.5). See table in HOW SUPPLIED for characteristics. Sodium Chloride, USP, chemically designated NaCl, is a white crystalline compound freely soluble in water."
    },
    {
      "NDCCode": "50114-0104-6",
      "PackageDescription": "10 AMPULE in 1 CARTON (50114-0104-6)  > 2.2 mL in 1 AMPULE",
      "NDC11Code": "50114-0104-06",
      "ProductNDC": "50114-0104",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Tonsilla Compositum",
      "NonProprietaryName": "Conium Maculatum Flowering Top, Solanum Dulcamara Top, Echinacea, Unspecified, Horse Chestnut,antimony Potassium Tartrate, Ascorbic Acid, Protortonia Cacti,galium Aparine,gentiana Lutea Root,geranium Robertianum, Pulsatilla Vulgaris,lactic Acid, L-, Sus Scrofa Adrenal Gland,sulfur,tribasic Calcium Phosphate,ferrosoferric Phosphate,sus Scrofa Umbilical Cord,pork Liver,sus Scrofa Hypothalamussus Scrofa Bone Marrow,sus Scrofa Spleen,sus Scrofa Adrenal Gland, Cortisone Acetate, Sus Scrofa Embryo,",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "CONIUM MACULATUM FLOWERING TOP; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; HORSE CHESTNUT; ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; PROTORTONIA CACTI; GALIUM APARINE; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; PULSATILLA VULGARIS; LACTIC ACID, L-; SULFUR; TRIBASIC CALCIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; SUS SCROFA ADRENAL GLAND; CORTISONE ACETATE; SUS SCROFA EMBRYO; MERCURIUS SOLUBILIS; LEVOTHYROXINE; BARIUM CARBONATE; SUS SCROFA TONSIL",
      "StrengthNumber": "4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 10; 10; 10; 10; 10; 10; 10; 13; 13; 13; 13; 13; 28; 28",
      "StrengthUnit": "[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; 1/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL",
      "Pharm_Classes": "Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]",
      "Status": "Deprecated",
      "LastUpdate": "2017-01-30"
    },
    {
      "NDCCode": "50114-0110-6",
      "PackageDescription": "10 VIAL in 1 CARTON (50114-0110-6)  > 2.2 mL in 1 VIAL",
      "NDC11Code": "50114-0110-06",
      "ProductNDC": "50114-0110",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Solidago Compositum",
      "NonProprietaryName": "Solidago Virgaurea Flowering Top And Baptisia Tinctoria Root And Berberis Vulgaris Root Bark And Equisetum Hyemale And Silver Nitrate And Lytta Vesicatoria And Capsicum And Cupric Sulfate And Clerodendranthus Spicatus Leaf And Chondrodendron Tomentosum Root And Smilax Regelii Root And Turpentine Oil And Apis Mellifera Venom And Agathosma Betulina Leaf And Human Coxsackievirus A And Mercuric Chloride And Sus Scrofa Urinary Bladder And Calcium Sulfide And Sodium Pyruvate",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "SOLIDAGO VIRGAUREA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; EQUISETUM HYEMALE; SILVER NITRATE; LYTTA VESICATORIA; CAPSICUM; CUPRIC SULFATE; CLERODENDRANTHUS SPICATUS LEAF; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX REGELII ROOT; TURPENTINE OIL; APIS MELLIFERA VENOM; AGATHOSMA BETULINA LEAF; HUMAN COXSACKIEVIRUS A; MERCURIC CHLORIDE; SUS SCROFA URINARY BLADDER; CALCIUM SULFIDE; SODIUM PYRUVATE; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; ESCHERICHIA COLI; ARSENIC TRIOXIDE",
      "StrengthNumber": "3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 13; 28",
      "StrengthUnit": "[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "50114-0113-6",
      "PackageDescription": "10 AMPULE in 1 CARTON (50114-0113-6)  > 2.2 mL in 1 AMPULE",
      "NDC11Code": "50114-0113-06",
      "ProductNDC": "50114-0113",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Echinacea Compositum Forte",
      "NonProprietaryName": "Aconitum Napellus,echinacea, Unspecified, Arnica Montana Root, Baptisia Tinctoria Root ,toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Euphorbia Resinifera Resin, Gelsemium Sempervirens Root, Phytolacca Americana Root, Silver Nitrate, Arsenic Trioxide, Mercuric Chloride, Phosphorus, Pulsatilla Vulgaris, Sulfur,thuja Occidentalis Leafy Twig,calcium Sulfide,lachesis Muta Venom,",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "ACONITUM NAPELLUS; ARNICA MONTANA ROOT; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CORTISONE ACETATE; ECHINACEA, UNSPECIFIED; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA RESINIFERA RESIN; GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS; LACHESIS MUTA VENOM; MERCURIC CHLORIDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; SANGUINARIA CANADENSIS ROOT; SILVER NITRATE; STAPHYLOCOCCUS EPIDERMIDIS; STAPHYLOCOCCUS HAEMOLYTICUS; STAPHYLOCOCCUS SIMULANS; STREPTOCOCCUS PYOGENES; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; ZINC",
      "StrengthNumber": "5; 6; 10; 6; 8; 12; 15; 3; 8; 8; 8; 15; 12; 8; 10; 8; 10; 6; 10; 20; 20; 20; 20; 10; 10; 6; 12",
      "StrengthUnit": "[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL",
      "Pharm_Classes": "Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2014-08-22"
    },
    {
      "NDCCode": "50114-0114-2",
      "PackageDescription": "10 VIAL, SINGLE-DOSE in 1 CARTON (50114-0114-2)  > .45 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "50114-0114-02",
      "ProductNDC": "50114-0114",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Oculoheel",
      "NonProprietaryName": "Cochlearia Officinalis Flowering Top,echinacea Angustifolia,euphrasia Stricta And Pilocarpus Jaborandi Leaf",
      "DosageFormName": "SOLUTION/ DROPS",
      "RouteName": "INTRAOCULAR",
      "StartMarketingDate": "20050627",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "COCHLEARIA OFFICINALIS FLOWERING TOP; ECHINACEA, UNSPECIFIED; EUPHRASIA STRICTA; PILOCARPUS JABORANDI LEAF",
      "StrengthNumber": "5; 5; 5; 5",
      "StrengthUnit": "[hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL",
      "Status": "Deprecated",
      "LastUpdate": "2017-01-30"
    },
    {
      "NDCCode": "50114-0119-2",
      "PackageDescription": "15 VIAL, SINGLE-DOSE in 1 CARTON (50114-0119-2)  > .45 mL in 1 VIAL, SINGLE-DOSE",
      "NDC11Code": "50114-0119-02",
      "ProductNDC": "50114-0119",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Clearlife",
      "NonProprietaryName": "Cochlearia Officinalis Flowering Top, Echinacea, Unspecified, Euphrasia Stricta And Pilocarpus Jaborandi Leaf",
      "DosageFormName": "SOLUTION/ DROPS",
      "RouteName": "OPHTHALMIC",
      "StartMarketingDate": "20130404",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "COCHLEARIA OFFICINALIS FLOWERING TOP; ECHINACEA, UNSPECIFIED; EUPHRASIA STRICTA; PILOCARPUS JABORANDI LEAF",
      "StrengthNumber": "5; 5; 5; 5",
      "StrengthUnit": "[hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-08-29"
    },
    {
      "NDCCode": "50114-0150-9",
      "PackageDescription": "1 BOTTLE, PUMP in 1 CARTON (50114-0150-9)  > 20 mL in 1 BOTTLE, PUMP",
      "NDC11Code": "50114-0150-09",
      "ProductNDC": "50114-0150",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Luffeel",
      "NonProprietaryName": "Galphimia Glauca Flowering Top And Histamine Dihydrochloride And Luffa Operculata Fruit And Sulfur",
      "DosageFormName": "SPRAY",
      "RouteName": "NASAL",
      "StartMarketingDate": "20110705",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR",
      "StrengthNumber": "4; 12; 4; 12",
      "StrengthUnit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
      "Status": "Deprecated",
      "LastUpdate": "2017-02-03"
    },
    {
      "NDCCode": "50114-0152-9",
      "PackageDescription": "1 BOTTLE, PUMP in 1 CARTON (50114-0152-9)  > 20 mL in 1 BOTTLE, PUMP",
      "NDC11Code": "50114-0152-09",
      "ProductNDC": "50114-0152",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Clearlife",
      "NonProprietaryName": "Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit And Sulfur",
      "DosageFormName": "SPRAY",
      "RouteName": "NASAL",
      "StartMarketingDate": "20130411",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR",
      "StrengthNumber": "4; 12; 4; 12",
      "StrengthUnit": "[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-08-29"
    },
    {
      "NDCCode": "50114-0227-2",
      "PackageDescription": "30000 mg in 1 BOTTLE (50114-0227-2)",
      "NDC11Code": "50114-0227-02",
      "ProductNDC": "50114-0227",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Atropinum Compositum Rx",
      "NonProprietaryName": "Atropine Sulfate And Bryonia Alba Root And Arsenic Trioxide And Berberis Vulgaris Root Bark And Citrullus Colocynthis Fruit Pulp And Cupric Acetate And Chondrodendron Tomentosum Root And Veratrum Album Root And Baptisia Tinctoria Root And Chelidonium Majus And Lytta Vesicatoria And Gonorrheal Urethral Secretion Human And Clematis Recta Flowering Top And Thuja Occidentalis Leafy Twig And Benzoic Acid And Silver Nitrate",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20030830",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "ATROPINE SULFATE; BRYONIA ALBA ROOT; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; CHONDRODENDRON TOMENTOSUM ROOT; VERATRUM ALBUM ROOT; BAPTISIA TINCTORIA ROOT; CHELIDONIUM MAJUS; LYTTA VESICATORIA; GONORRHEAL URETHRAL SECRETION HUMAN; CLEMATIS RECTA FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; BENZOIC ACID; SILVER NITRATE",
      "StrengthNumber": "4; 1; 4; 1; 1; 2; 1; 1; 1; 1; 5; 10; 1; 1; 2; 1",
      "StrengthUnit": "[hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg",
      "Pharm_Classes": "Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2017-04-04"
    },
    {
      "NDCCode": "50114-0988-4",
      "PackageDescription": "50 mL in 1 BOTTLE (50114-0988-4)",
      "NDC11Code": "50114-0988-04",
      "ProductNDC": "50114-0988",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Anacardium Homaccord",
      "NonProprietaryName": "Semecarpus Anacardium Juice And Iodine And Ipecac",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "19860131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "SEMECARPUS ANACARDIUM JUICE; IODINE; IPECAC",
      "StrengthNumber": "6; 30; 4",
      "StrengthUnit": "[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2017-02-24"
    },
    {
      "NDCCode": "50114-1000-4",
      "PackageDescription": "50 mL in 1 BOTTLE (50114-1000-4)",
      "NDC11Code": "50114-1000-04",
      "ProductNDC": "50114-1000",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Aesculus Compositum",
      "NonProprietaryName": "Horse Chestnut And Echinacea Pallida And Arnica Montana Root And Claviceps Purpurea Sclerotium And Viscum Album Whole And Apis Mellifera And Baptisia Tinctoria Root And Benzoic Acid And Colchicum Autu",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "19860131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "APIS MELLIFERA; ARNICA MONTANA ROOT; BAPTISIA TINCTORIA ROOT; BARIUM IODIDE; BENZOIC ACID; CLAVICEPS PURPUREA SCLEROTIUM; COLCHICUM AUTUMNALE BULB; COPPER; ECHINACEA PALLIDA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HORSE CHESTNUT; LEAD IODIDE; RUTA GRAVEOLENS FLOWERING TOP; SOLANUM DULCAMARA STEM; SOLANUM NIGRUM WHOLE; TOBACCO LEAF; TOXICODENDRON PUBESCENS LEAF; VISCUM ALBUM WHOLE",
      "StrengthNumber": "4; 3; 4; 6; 4; 3; 4; 13; 2; 4; 1; 20; 4; 4; 6; 10; 4; 3",
      "StrengthUnit": "[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-08-29"
    },
    {
      "NDCCode": "50114-1010-4",
      "PackageDescription": "50 mL in 1 BOTTLE (50114-1010-4)",
      "NDC11Code": "50114-1010-04",
      "ProductNDC": "50114-1010",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Arnica-heel",
      "NonProprietaryName": "Apis Mellifera And Baptisia Tinctoria Root And Solanum Dulcamara Stem And Eucalyptus Globulus Leaf And Solanum Nigrum Whole And Toxicodendron Pubescens Leaf And Eupatorium Cannabinum And Arnica Montan",
      "DosageFormName": "LIQUID",
      "RouteName": "ORAL",
      "StartMarketingDate": "19860131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "APIS MELLIFERA; ARNICA MONTANA ROOT; BAPTISIA TINCTORIA ROOT; BENZOIC ACID; BRYONIA ALBA ROOT; COLCHICUM AUTUMNALE BULB; ECHINACEA, UNSPECIFIED; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM CANNABINUM; MERCURIALIS PERENNIS; SOLANUM DULCAMARA STEM; SOLANUM LYCOPERSICUM; SOLANUM NIGRUM WHOLE; TOXICODENDRON PUBESCENS LEAF",
      "StrengthNumber": "4; 3; 4; 3; 4; 4; 3; 4; 2; 3; 4; 3; 4; 6",
      "StrengthUnit": "[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-11-21"
    },
    {
      "NDCCode": "50114-1032-6",
      "PackageDescription": "10 VIAL in 1 CARTON (50114-1032-6)  > 1.1 mL in 1 VIAL",
      "NDC11Code": "50114-1032-06",
      "ProductNDC": "50114-1032",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Cimicifuga-homaccord",
      "NonProprietaryName": "Black Cohosh And Strontium Carbonate",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "BLACK COHOSH; STRONTIUM CARBONATE",
      "StrengthNumber": "4; 8",
      "StrengthUnit": "[hp_X]/1.1mL; [hp_X]/1.1mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-11-21"
    },
    {
      "NDCCode": "50114-1034-6",
      "PackageDescription": "10 VIAL in 1 CARTON (50114-1034-6)  > 1.1 mL in 1 VIAL",
      "NDC11Code": "50114-1034-06",
      "ProductNDC": "50114-1034",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Colocynthis-homaccord",
      "NonProprietaryName": "Citrullus Colocynthis Fruit Pulp And Pseudognaphalium Obtusifolium",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": "CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM",
      "StrengthNumber": "4; 3",
      "StrengthUnit": "[hp_X]/1.1mL; [hp_X]/1.1mL",
      "Status": "Deprecated",
      "LastUpdate": "2015-06-26"
    },
    {
      "NDCCode": "50114-1058-6",
      "PackageDescription": "10 AMPULE in 1 CARTON (50114-1058-6)  > 2.2 mL in 1 AMPULE",
      "NDC11Code": "50114-1058-06",
      "ProductNDC": "50114-1058",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Cor Compositum",
      "NonProprietaryName": "Selenicereus Grandiflorus Stem, Arnica Montana Root, Nitroglycerin,potassium Carbonate, Kalmia Latifolia Leaf, Crataegus Laevigata Fruit,strychnos Ignatii Seed, Ranunculus Bulbosus, Lactic Acid, L-,arsenic Trioxide, Pork Heart, Fumaric Acid, Pork Liver,.alpha.-ketoglutaric Acid, Malic Acid, Sodium Diethyl Oxalacetate, Ouabain, Naja Naja Venom,spigelia Anthelmia And Activated Charcoal",
      "DosageFormName": "SOLUTION",
      "RouteName": "ORAL",
      "StartMarketingDate": "19930131",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Heel Inc",
      "SubstanceName": ".ALPHA.-KETOGLUTARIC ACID; ACTIVATED CHARCOAL; ARNICA MONTANA ROOT; ARSENIC TRIOXIDE; CRATAEGUS LAEVIGATA FRUIT; FUMARIC ACID; KALMIA LATIFOLIA LEAF; LACTIC ACID, L-; MALIC ACID; NAJA NAJA VENOM; NITROGLYCERIN; OUABAIN; PORK HEART; PORK LIVER; POTASSIUM CARBONATE; RANUNCULUS BULBOSUS; SELENICEREUS GRANDIFLORUS STEM; SPIGELIA ANTHELMIA; STRYCHNOS IGNATII SEED",
      "StrengthNumber": "8; 18; 4; 8; 6; 8; 4; 6; 8; 10; 4; 8; 8; 8; 4; 6; 3; 10; 6",
      "StrengthUnit": "[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL",
      "Pharm_Classes": "Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]",
      "Status": "Deprecated",
      "LastUpdate": "2014-08-22"
    }
  ]
}
                    

{"NDC":[{"NDCCode":"50114-7026-1","ProprietaryName":"Lymphomyosot","NonProprietaryName":"Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine"},{"NDCCode":"50114-7026-2","ProprietaryName":"Lymphomyosot","NonProprietaryName":"Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine"},{"NDCCode":"0002-7026-60","ProprietaryName":"Jaypirca","NonProprietaryName":"Pirtobrutinib"},{"NDCCode":"0002-7026-99","ProprietaryName":"Jaypirca","NonProprietaryName":"Pirtobrutinib"},{"NDCCode":"0338-7026-06","ProprietaryName":"Clinimix E","NonProprietaryName":"Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose"},{"NDCCode":"0440-7026-30","ProprietaryName":"Acetaminophen And Codeine","NonProprietaryName":"Acetaminophen And Codeine Phosphate"},{"NDCCode":"0440-7026-40","ProprietaryName":"Acetaminophen And Codeine","NonProprietaryName":"Acetaminophen And Codeine Phosphate"},{"NDCCode":"0904-7026-61","ProprietaryName":"Nitrofurantoin Macrocrystals","NonProprietaryName":"Nitrofurantoin Macrocrystals"},{"NDCCode":"10888-7026-1","NonProprietaryName":"Docusate Sodium"},{"NDCCode":"50090-7026-1","ProprietaryName":"Cephalexin","NonProprietaryName":"Cephalexin"},{"NDCCode":"50090-7026-3","ProprietaryName":"Cephalexin","NonProprietaryName":"Cephalexin"},{"NDCCode":"52731-7026-2","ProprietaryName":"Air Pollution Complex","NonProprietaryName":"Arnica Montana 6x, Bovista 6x, Calcarea Carbonica 8x,carbo Vegetabilis 8x, Cicuta Virosa 6x, Euphorbium Officinarum 6x,hydrastis Canadensis 4x, Petroleum 6x, Phosphorus 8x, Plumbum Metallicum 8x, Sulf"},{"NDCCode":"62670-7026-0","ProprietaryName":"Anti Bacterial Hand Gel","NonProprietaryName":"Alcohol"},{"NDCCode":"68788-7026-3","ProprietaryName":"Levothyroxine Sodium","NonProprietaryName":"Levothyroxine Sodium"},{"NDCCode":"68788-7026-9","ProprietaryName":"Levothyroxine Sodium","NonProprietaryName":"Levothyroxine Sodium"},{"NDCCode":"71872-7026-1","ProprietaryName":"Quelicin","NonProprietaryName":"Succinylcholine Chloride"},{"NDCCode":"50114-0104-6","ProprietaryName":"Tonsilla Compositum","NonProprietaryName":"Conium Maculatum Flowering Top, Solanum Dulcamara Top, Echinacea, Unspecified, Horse Chestnut,antimony Potassium Tartrate, Ascorbic Acid, Protortonia Cacti,galium Aparine,gentiana Lutea Root,geranium Robertianum, Pulsatilla Vulgaris,lactic Acid, L-, Sus Scrofa Adrenal Gland,sulfur,tribasic Calcium Phosphate,ferrosoferric Phosphate,sus Scrofa Umbilical Cord,pork Liver,sus Scrofa Hypothalamussus Scrofa Bone Marrow,sus Scrofa Spleen,sus Scrofa Adrenal Gland, Cortisone Acetate, Sus Scrofa Embryo,"},{"NDCCode":"50114-0110-6","ProprietaryName":"Solidago Compositum","NonProprietaryName":"Solidago Virgaurea Flowering Top And Baptisia Tinctoria Root And Berberis Vulgaris Root Bark And Equisetum Hyemale And Silver Nitrate And Lytta Vesicatoria And Capsicum And Cupric Sulfate And Clerodendranthus Spicatus Leaf And Chondrodendron Tomentosum Root And Smilax Regelii Root And Turpentine Oil And Apis Mellifera Venom And Agathosma Betulina Leaf And Human Coxsackievirus A And Mercuric Chloride And Sus Scrofa Urinary Bladder And Calcium Sulfide And Sodium Pyruvate"},{"NDCCode":"50114-0113-6","ProprietaryName":"Echinacea Compositum Forte","NonProprietaryName":"Aconitum Napellus,echinacea, Unspecified, Arnica Montana Root, Baptisia Tinctoria Root ,toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Euphorbia Resinifera Resin, Gelsemium Sempervirens Root, Phytolacca Americana Root, Silver Nitrate, Arsenic Trioxide, Mercuric Chloride, Phosphorus, Pulsatilla Vulgaris, Sulfur,thuja Occidentalis Leafy Twig,calcium Sulfide,lachesis Muta Venom,"},{"NDCCode":"50114-0114-2","ProprietaryName":"Oculoheel","NonProprietaryName":"Cochlearia Officinalis Flowering Top,echinacea Angustifolia,euphrasia Stricta And Pilocarpus Jaborandi Leaf"},{"NDCCode":"50114-0119-2","ProprietaryName":"Clearlife","NonProprietaryName":"Cochlearia Officinalis Flowering Top, Echinacea, Unspecified, Euphrasia Stricta And Pilocarpus Jaborandi Leaf"},{"NDCCode":"50114-0150-9","ProprietaryName":"Luffeel","NonProprietaryName":"Galphimia Glauca Flowering Top And Histamine Dihydrochloride And Luffa Operculata Fruit And Sulfur"},{"NDCCode":"50114-0152-9","ProprietaryName":"Clearlife","NonProprietaryName":"Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit And Sulfur"},{"NDCCode":"50114-0227-2","ProprietaryName":"Atropinum Compositum Rx","NonProprietaryName":"Atropine Sulfate And Bryonia Alba Root And Arsenic Trioxide And Berberis Vulgaris Root Bark And Citrullus Colocynthis Fruit Pulp And Cupric Acetate And Chondrodendron Tomentosum Root And Veratrum Album Root And Baptisia Tinctoria Root And Chelidonium Majus And Lytta Vesicatoria And Gonorrheal Urethral Secretion Human And Clematis Recta Flowering Top And Thuja Occidentalis Leafy Twig And Benzoic Acid And Silver Nitrate"},{"NDCCode":"50114-0988-4","ProprietaryName":"Anacardium Homaccord","NonProprietaryName":"Semecarpus Anacardium Juice And Iodine And Ipecac"},{"NDCCode":"50114-1000-4","ProprietaryName":"Aesculus Compositum","NonProprietaryName":"Horse Chestnut And Echinacea Pallida And Arnica Montana Root And Claviceps Purpurea Sclerotium And Viscum Album Whole And Apis Mellifera And Baptisia Tinctoria Root And Benzoic Acid And Colchicum Autu"},{"NDCCode":"50114-1010-4","ProprietaryName":"Arnica-heel","NonProprietaryName":"Apis Mellifera And Baptisia Tinctoria Root And Solanum Dulcamara Stem And Eucalyptus Globulus Leaf And Solanum Nigrum Whole And Toxicodendron Pubescens Leaf And Eupatorium Cannabinum And Arnica Montan"},{"NDCCode":"50114-1032-6","ProprietaryName":"Cimicifuga-homaccord","NonProprietaryName":"Black Cohosh And Strontium Carbonate"},{"NDCCode":"50114-1034-6","ProprietaryName":"Colocynthis-homaccord","NonProprietaryName":"Citrullus Colocynthis Fruit Pulp And Pseudognaphalium Obtusifolium"},{"NDCCode":"50114-1058-6","ProprietaryName":"Cor Compositum","NonProprietaryName":"Selenicereus Grandiflorus Stem, Arnica Montana Root, Nitroglycerin,potassium Carbonate, Kalmia Latifolia Leaf, Crataegus Laevigata Fruit,strychnos Ignatii Seed, Ranunculus Bulbosus, Lactic Acid, L-,arsenic Trioxide, Pork Heart, Fumaric Acid, Pork Liver,.alpha.-ketoglutaric Acid, Malic Acid, Sodium Diethyl Oxalacetate, Ouabain, Naja Naja Venom,spigelia Anthelmia And Activated Charcoal"}]}
                    

<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <NDC>
    <NDCCode>50114-7026-1</NDCCode>
    <PackageDescription>10 AMPULE in 1 CARTON (50114-7026-1)  &gt; 1.1 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>50114-7026-01</NDC11Code>
    <ProductNDC>50114-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Lymphomyosot</ProprietaryName>
    <NonProprietaryName>Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20100401</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>ARANEUS DIADEMATUS; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; LEVOTHYROXINE; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SMILAX REGELII ROOT; SODIUM SULFATE; TEUCRIUM SCORODONIA FLOWERING TOP; TRIBASIC CALCIUM PHOSPHATE; VERONICA OFFICINALIS FLOWERING TOP</SubstanceName>
    <StrengthNumber>6; 4; 12; 4; 5; 4; 3; 3; 12; 3; 4; 4; 3; 6; 4; 3; 12; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL</StrengthUnit>
    <Pharm_Classes>l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2015-01-16</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-7026-2</NDCCode>
    <PackageDescription>1 AMPULE in 1 CARTON (50114-7026-2)  &gt; 1.1 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>50114-7026-02</NDC11Code>
    <ProductNDC>50114-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Lymphomyosot</ProprietaryName>
    <NonProprietaryName>Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20100401</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>ARANEUS DIADEMATUS; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; LEVOTHYROXINE; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; PINUS SYLVESTRIS FLOWERING TOP; SCROPHULARIA NODOSA; SMILAX REGELII ROOT; SODIUM SULFATE; TEUCRIUM SCORODONIA FLOWERING TOP; TRIBASIC CALCIUM PHOSPHATE; VERONICA OFFICINALIS FLOWERING TOP</SubstanceName>
    <StrengthNumber>6; 4; 12; 4; 5; 4; 3; 3; 12; 3; 4; 4; 3; 6; 4; 3; 12; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL</StrengthUnit>
    <Pharm_Classes>l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2015-01-16</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>0002-7026-60</NDCCode>
    <PackageDescription>60 TABLET, COATED in 1 BOTTLE (0002-7026-60) </PackageDescription>
    <NDC11Code>00002-7026-60</NDC11Code>
    <ProductNDC>0002-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Jaypirca</ProprietaryName>
    <NonProprietaryName>Pirtobrutinib</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20230127</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA216059</ApplicationNumber>
    <LabelerName>Eli Lilly and Company</LabelerName>
    <SubstanceName>PIRTOBRUTINIB</SubstanceName>
    <StrengthNumber>100</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Breast Cancer Resistance Protein Inhibitors [MoA], Bruton's Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-03-24</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230127</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>JAYPIRCA® is a kinase inhibitor indicated for the treatment of: : 1 Adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two lines of systemic therapy, including a BTK inhibitor. (1.1).This indication is approved under accelerated approval based on response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. , 2 Adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent BTK inhibitor. (1.2).</IndicationAndUsage>
    <Description>Pirtobrutinib is a kinase inhibitor. It is an orally available, small molecule ATP-competitive inhibitor of BTK. The active pharmaceutical ingredient is pirtobrutinib with the molecular formula C22H21F4N5O3 and a molecular weight of 479.44 g/mol. The chemical name for pirtobrutinib is 5-amino-3-{4-[(5-fluoro-2-methoxybenzamido)methyl]phenyl}-1-[(2S)-1,1,1-trifluoropropan-2-yl]-1H-pyrazole-4-carboxamide. Pirtobrutinib is a white to practically white to yellow to brown solid. The aqueous solubility of pirtobrutinib is considered practically insoluble, or insoluble, across the pH 1 to pH 7 range. Pirtobrutinib tablets are supplied as 50 mg or 100 mg film-coated, debossed tablets for oral administration. Each tablet contains inactive ingredients of croscarmellose sodium, hypromellose acetate succinate, lactose monohydrate, magnesium stearate, microcrystalline cellulose and silicon dioxide. The tablet film coating material contains FD&amp;C Blue #2, hypromellose, titanium dioxide and triacetin.</Description>
  </NDC>
  <NDC>
    <NDCCode>0002-7026-99</NDCCode>
    <PackageDescription>30 TABLET, COATED in 1 BOTTLE (0002-7026-99) </PackageDescription>
    <NDC11Code>00002-7026-99</NDC11Code>
    <ProductNDC>0002-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Jaypirca</ProprietaryName>
    <NonProprietaryName>Pirtobrutinib</NonProprietaryName>
    <DosageFormName>TABLET, COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20230127</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA216059</ApplicationNumber>
    <LabelerName>Eli Lilly and Company</LabelerName>
    <SubstanceName>PIRTOBRUTINIB</SubstanceName>
    <StrengthNumber>100</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Breast Cancer Resistance Protein Inhibitors [MoA], Bruton's Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-03-24</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20230215</StartMarketingDatePackage>
    <SamplePackage>Y</SamplePackage>
    <IndicationAndUsage>JAYPIRCA® is a kinase inhibitor indicated for the treatment of: : 1 Adult patients with relapsed or refractory mantle cell lymphoma (MCL) after at least two lines of systemic therapy, including a BTK inhibitor. (1.1).This indication is approved under accelerated approval based on response rate. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial. , 2 Adult patients with relapsed or refractory chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) who have previously been treated with a covalent BTK inhibitor. (1.2).</IndicationAndUsage>
    <Description>Pirtobrutinib is a kinase inhibitor. It is an orally available, small molecule ATP-competitive inhibitor of BTK. The active pharmaceutical ingredient is pirtobrutinib with the molecular formula C22H21F4N5O3 and a molecular weight of 479.44 g/mol. The chemical name for pirtobrutinib is 5-amino-3-{4-[(5-fluoro-2-methoxybenzamido)methyl]phenyl}-1-[(2S)-1,1,1-trifluoropropan-2-yl]-1H-pyrazole-4-carboxamide. Pirtobrutinib is a white to practically white to yellow to brown solid. The aqueous solubility of pirtobrutinib is considered practically insoluble, or insoluble, across the pH 1 to pH 7 range. Pirtobrutinib tablets are supplied as 50 mg or 100 mg film-coated, debossed tablets for oral administration. Each tablet contains inactive ingredients of croscarmellose sodium, hypromellose acetate succinate, lactose monohydrate, magnesium stearate, microcrystalline cellulose and silicon dioxide. The tablet film coating material contains FD&amp;C Blue #2, hypromellose, titanium dioxide and triacetin.</Description>
  </NDC>
  <NDC>
    <NDCCode>0338-7026-06</NDCCode>
    <PackageDescription>6 BAG in 1 CARTON (0338-7026-06)  / 1000 mL in 1 BAG (0338-7026-01) </PackageDescription>
    <NDC11Code>00338-7026-06</NDC11Code>
    <ProductNDC>0338-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Clinimix E</ProprietaryName>
    <NonProprietaryName>Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20240715</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA020678</ApplicationNumber>
    <LabelerName>Baxter Healthcare Company</LabelerName>
    <SubstanceName>LEUCINE; PHENYLALANINE; LYSINE; METHIONINE; ISOLEUCINE; VALINE; HISTIDINE; THREONINE; TRYPTOPHAN; ALANINE; GLYCINE; ARGININE; PROLINE; SERINE; TYROSINE; SODIUM ACETATE; POTASSIUM PHOSPHATE, DIBASIC; MAGNESIUM CHLORIDE; SODIUM CHLORIDE; CALCIUM CHLORIDE; DEXTROSE</SubstanceName>
    <StrengthNumber>311; 238; 247; 170; 255; 247; 204; 179; 77; 880; 438; 489; 289; 213; 17; 297; 261; 51; 77; 33; 10</StrengthNumber>
    <StrengthUnit>mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; mg/100mL; g/100mL</StrengthUnit>
    <Pharm_Classes>Amino Acid [EPC], Amino Acids [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-06-06</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240715</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>CLINIMIX E is indicated as a source of calories, protein, and electrolytes for patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated. CLINIMIX E may be used to treat negative nitrogen balance in patients.</IndicationAndUsage>
    <Description>CLINIMIX E sulfite-free (amino acids with electrolytes in dextrose with calcium) injection for intravenous use consists of sterile, nonpyrogenic, hypertonic solutions in a dual chamber container. The outlet port chamber contains essential and nonessential amino acids with electrolytes. The formulas for the individual electrolytes and amino acids are provided in Table 8. The injection port chamber contains dextrose with calcium. The formula for Calcium Chloride is: CaCl22H2O. Dextrose, USP, is chemically designated D-glucose, monohydrate (C6H12O6  H2O) and has the following structure. Dextrose is derived from corn. See Table 7 for composition, pH, osmolarity, ionic concentration and caloric content of the admixed product [see Dosage Forms and Strengths (3)]. The dual chamber container is a lipid-compatible plastic container (PL 2401 Plastic). CLINIMIX E contains no more than 25 mcg/L of aluminum.</Description>
  </NDC>
  <NDC>
    <NDCCode>0440-7026-30</NDCCode>
    <PackageDescription>30 TABLET in 1 BOTTLE, PLASTIC (0440-7026-30)</PackageDescription>
    <NDC11Code>00440-7026-30</NDC11Code>
    <ProductNDC>0440-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Acetaminophen And Codeine</ProprietaryName>
    <NonProprietaryName>Acetaminophen And Codeine Phosphate</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19880930</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA089805</ApplicationNumber>
    <LabelerName>Liberty Pharmaceuticals, Inc.</LabelerName>
    <SubstanceName>CODEINE PHOSPHATE; ACETAMINOPHEN</SubstanceName>
    <StrengthNumber>30; 300</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Full Opioid Agonists [MoA],Opioid Agonist [EPC]</Pharm_Classes>
    <DEASchedule>CIII</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain.</IndicationAndUsage>
    <Description>Acetaminophen and codeine is supplied in tablet form for oral administration. Acetaminophen, 4'-hydroxyacetanilide, a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. It has the following structural formula. Codeine phosphate, 7,8-didehydro-4,5α-epoxy-3-methoxy-17methylmorphinan-6α-ol phosphate (1:1) (salt) hemihydrate, a white crystalline powder, is a narcotic analgesic and antitussive. It has the following structural formula. Each 300 mg/30 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................30 mg. Each 300 mg/60 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................60 mg.</Description>
  </NDC>
  <NDC>
    <NDCCode>0440-7026-40</NDCCode>
    <PackageDescription>40 TABLET in 1 BOTTLE, PLASTIC (0440-7026-40)</PackageDescription>
    <NDC11Code>00440-7026-40</NDC11Code>
    <ProductNDC>0440-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Acetaminophen And Codeine</ProprietaryName>
    <NonProprietaryName>Acetaminophen And Codeine Phosphate</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19880930</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA089805</ApplicationNumber>
    <LabelerName>Liberty Pharmaceuticals, Inc.</LabelerName>
    <SubstanceName>CODEINE PHOSPHATE; ACETAMINOPHEN</SubstanceName>
    <StrengthNumber>30; 300</StrengthNumber>
    <StrengthUnit>mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Full Opioid Agonists [MoA],Opioid Agonist [EPC]</Pharm_Classes>
    <DEASchedule>CIII</DEASchedule>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Acetaminophen and codeine phosphate tablets are indicated for the relief of mild to moderately severe pain.</IndicationAndUsage>
    <Description>Acetaminophen and codeine is supplied in tablet form for oral administration. Acetaminophen, 4'-hydroxyacetanilide, a slightly bitter, white, odorless, crystalline powder, is a non-opiate, non-salicylate analgesic and antipyretic. It has the following structural formula. Codeine phosphate, 7,8-didehydro-4,5α-epoxy-3-methoxy-17methylmorphinan-6α-ol phosphate (1:1) (salt) hemihydrate, a white crystalline powder, is a narcotic analgesic and antitussive. It has the following structural formula. Each 300 mg/30 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................30 mg. Each 300 mg/60 mg Acetaminophen and Codeine Phosphate Tablet contains:          Acetaminophen ......................................................................................................300 mg          Codeine Phosphate ..................................................................................................60 mg.</Description>
  </NDC>
  <NDC>
    <NDCCode>0904-7026-61</NDCCode>
    <PackageDescription>100 BLISTER PACK in 1 CARTON (0904-7026-61)  / 1 CAPSULE in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>00904-7026-61</NDC11Code>
    <ProductNDC>0904-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Nitrofurantoin Macrocrystals</ProprietaryName>
    <NonProprietaryName>Nitrofurantoin Macrocrystals</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20180215</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA205005</ApplicationNumber>
    <LabelerName>Major Pharmaceuticals</LabelerName>
    <SubstanceName>NITROFURANTOIN</SubstanceName>
    <StrengthNumber>50</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Nitrofuran Antibacterial [EPC], Nitrofurans [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2026-03-24</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180215</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Nitrofurantoin macrocrystals capsules are specifically indicated for the treatment of urinary tract infections when due to susceptible strains of Escherichia coli, enterococci, Staphylococcus aureus, and certain susceptible strains of Klebsiella and Enterobacter species. Nitrofurantoin is not indicated for the treatment of pyelonephritis or perinephric abscesses. To reduce the development of drug-resistant bacteria and maintain the effectiveness of nitrofurantoin macrocrystals capsules and other antibacterial drugs, nitrofurantoin macrocrystals capsules should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Nitrofurantoins lack the broader tissue distribution of other therapeutic agents approved for urinary tract infections. Consequently, many patients who are treated with nitrofurantoin macrocrystals capsules are predisposed to persistence or reappearance of bacteriuria. Urine specimens for culture and susceptibility testing should be obtained before and after completion of therapy. If persistence or reappearance of bacteriuria occurs after treatment with nitrofurantoin macrocrystals capsules, other therapeutic agents with broader tissue distribution should be selected. In considering the use of nitrofurantoin macrocrystals capsules, lower eradication rates should be balanced against the increased potential for systemic toxicity and for the development of antimicrobial resistance when agents with broader tissue distribution are utilized.</IndicationAndUsage>
    <Description>Nitrofurantoin capsules, USP (macrocrystals) is a synthetic chemical of controlled crystal size. It is a stable, lemon-yellow, crystalline compound. Nitrofurantoin capsules, USP (macrocrystals) is an antibacterial agent for specific urinary tract infections. It is available in 50 mg and 100 mg capsules for oral administration. 1-[[(5-nitro-2-furanyl)methylene] amino]-2,4-imidazolidinedione. Nitrofurantoin macrocrystals is a lemon-yellow crystalline compound. It is soluble in dimethylformamide, very slightly soluble in water and in alcohol. Each nitrofurantoin capsules, USP (macrocrystals) intended for oral administration contains 50 mg and 100 mg of nitrofurantoin macrocrystals. In addition, each capsule contains the following inactive ingredients: gelatin, lactose monohydrate, magnesium stearate, pregelatinized starch, talc and titanium dioxide. Additionally each 50 mg and 100 mg capsule shell contains FD &amp; C Blue # 1, FD &amp; C Red # 3 and sodium lauryl sulphate. The capsule is printed with black pharmaceutical ink which contains black iron oxide, potassium hydroxide, propylene glycol and shellac.</Description>
  </NDC>
  <NDC>
    <NDCCode>10888-7026-1</NDCCode>
    <PackageDescription>18000 CAPSULE, LIQUID FILLED in 1 CARTON (10888-7026-1)</PackageDescription>
    <NDC11Code>10888-7026-01</NDC11Code>
    <ProductNDC>10888-7026</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Docusate Sodium</NonProprietaryName>
    <DosageFormName>CAPSULE, LIQUID FILLED</DosageFormName>
    <StartMarketingDate>20110701</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Banner Pharmacaps Inc</LabelerName>
    <SubstanceName>DOCUSATE SODIUM</SubstanceName>
    <StrengthNumber>100</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>50090-7026-1</NDCCode>
    <PackageDescription>12 CAPSULE in 1 BOTTLE (50090-7026-1) </PackageDescription>
    <NDC11Code>50090-7026-01</NDC11Code>
    <ProductNDC>50090-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Cephalexin</ProprietaryName>
    <NonProprietaryName>Cephalexin</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151019</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA090836</ApplicationNumber>
    <LabelerName>A-S Medication Solutions</LabelerName>
    <SubstanceName>CEPHALEXIN</SubstanceName>
    <StrengthNumber>500</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Cephalosporin Antibacterial [EPC], Cephalosporins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-07-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240108</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Cephalexin is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria: 1 Respiratory tract infection (1.1), 2 Otitis media (1.2), 3 Skin and skin structure infections (1.3), 4 Bone infections (1.4), 5 Genitourinary tract infections (1.5).</IndicationAndUsage>
    <Description>Cephalexin capsules, USP is a semisynthetic cephalosporin antibacterial drug intended for oral administration. It is 7-(D-α-Amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate. Cephalexin has the molecular formula C 16H 17N 3O 4SH 2O and the molecular weight is 365.41. Cephalexin has the following structural formula. Each capsule contains cephalexin monohydrate equivalent to 250 mg, 333 mg, 500 mg, or 750 mg of cephalexin. The 250 mg, 333 mg, 500 mg and 750 mg capsules contain anhydrous lactose, colloidal silicon dioxide, magnesium stearate, FD &amp; C Blue No. 1, D &amp; C Yellow No. 10, gelatin, sodium lauryl sulphate, titanium dioxide. In addition, the 250 mg capsule contains FD &amp; C Red No. 40; 333 mg and 750 mg Capsules contains FD &amp; C Yellow No. 6. The imprinting ink contains; shellac, propylene glycol, strong ammonia solution and potassium hydroxide. Also black Iron oxide is used in 250 mg, 333 mg and 500 mg and titanium dioxide is used in 750 mg.</Description>
  </NDC>
  <NDC>
    <NDCCode>50090-7026-3</NDCCode>
    <PackageDescription>6 CAPSULE in 1 BOTTLE (50090-7026-3) </PackageDescription>
    <NDC11Code>50090-7026-03</NDC11Code>
    <ProductNDC>50090-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Cephalexin</ProprietaryName>
    <NonProprietaryName>Cephalexin</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20151019</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA090836</ApplicationNumber>
    <LabelerName>A-S Medication Solutions</LabelerName>
    <SubstanceName>CEPHALEXIN</SubstanceName>
    <StrengthNumber>500</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Cephalosporin Antibacterial [EPC], Cephalosporins [CS]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2024-07-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240108</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Cephalexin is a cephalosporin antibacterial drug indicated for the treatment of the following infections caused by susceptible isolates of designated bacteria: 1 Respiratory tract infection (1.1), 2 Otitis media (1.2), 3 Skin and skin structure infections (1.3), 4 Bone infections (1.4), 5 Genitourinary tract infections (1.5).</IndicationAndUsage>
    <Description>Cephalexin capsules, USP is a semisynthetic cephalosporin antibacterial drug intended for oral administration. It is 7-(D-α-Amino-α-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid monohydrate. Cephalexin has the molecular formula C 16H 17N 3O 4SH 2O and the molecular weight is 365.41. Cephalexin has the following structural formula. Each capsule contains cephalexin monohydrate equivalent to 250 mg, 333 mg, 500 mg, or 750 mg of cephalexin. The 250 mg, 333 mg, 500 mg and 750 mg capsules contain anhydrous lactose, colloidal silicon dioxide, magnesium stearate, FD &amp; C Blue No. 1, D &amp; C Yellow No. 10, gelatin, sodium lauryl sulphate, titanium dioxide. In addition, the 250 mg capsule contains FD &amp; C Red No. 40; 333 mg and 750 mg Capsules contains FD &amp; C Yellow No. 6. The imprinting ink contains; shellac, propylene glycol, strong ammonia solution and potassium hydroxide. Also black Iron oxide is used in 250 mg, 333 mg and 500 mg and titanium dioxide is used in 750 mg.</Description>
  </NDC>
  <NDC>
    <NDCCode>52731-7026-2</NDCCode>
    <PackageDescription>1 BOTTLE in 1 BOX (52731-7026-2)  &gt; 50 mL in 1 BOTTLE (52731-7026-1)</PackageDescription>
    <NDC11Code>52731-7026-02</NDC11Code>
    <ProductNDC>52731-7026</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Air Pollution Complex</ProprietaryName>
    <NonProprietaryName>Arnica Montana 6x, Bovista 6x, Calcarea Carbonica 8x,carbo Vegetabilis 8x, Cicuta Virosa 6x, Euphorbium Officinarum 6x,hydrastis Canadensis 4x, Petroleum 6x, Phosphorus 8x, Plumbum Metallicum 8x, Sulf</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20110601</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Nova Homeopathic Therapeutics, Inc.</LabelerName>
    <SubstanceName>ARNICA MONTANA; GIANT PUFFBALL; OYSTER SHELL CALCIUM CARBONATE, CRUDE; ACTIVATED CHARCOAL; CICUTA VIROSA ROOT; EUPHORBIA RESINIFERA RESIN; GOLDENSEAL; LIQUID PETROLEUM; PHOSPHORUS; LEAD; SULFUR</SubstanceName>
    <StrengthNumber>6; 6; 8; 8; 6; 6; 4; 6; 8; 8; 30</StrengthNumber>
    <StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>For oral use only.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>62670-7026-0</NDCCode>
    <PackageDescription>29 mL in 1 BOTTLE (62670-7026-0) </PackageDescription>
    <NDC11Code>62670-7026-00</NDC11Code>
    <ProductNDC>62670-7026</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Anti Bacterial Hand Gel</ProprietaryName>
    <ProprietaryNameSuffix>Waikiki Beach Coconut</ProprietaryNameSuffix>
    <NonProprietaryName>Alcohol</NonProprietaryName>
    <DosageFormName>GEL</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20260209</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>505G(a)(3)</ApplicationNumber>
    <LabelerName>Bath &amp; Body Works, Inc.</LabelerName>
    <SubstanceName>ALCOHOL</SubstanceName>
    <StrengthNumber>71</StrengthNumber>
    <StrengthUnit>mL/100mL</StrengthUnit>
    <Status>Active</Status>
    <LastUpdate>2026-07-03</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20260209</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Decreases bacteria on hands.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>68788-7026-3</NDCCode>
    <PackageDescription>30 TABLET in 1 BOTTLE (68788-7026-3) </PackageDescription>
    <NDC11Code>68788-7026-03</NDC11Code>
    <ProductNDC>68788-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Levothyroxine Sodium</ProprietaryName>
    <NonProprietaryName>Levothyroxine Sodium</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20171012</StartMarketingDate>
    <MarketingCategoryName>NDA AUTHORIZED GENERIC</MarketingCategoryName>
    <ApplicationNumber>NDA021342</ApplicationNumber>
    <LabelerName>Preferrred Pharmaeuticals Inc.</LabelerName>
    <SubstanceName>LEVOTHYROXINE SODIUM</SubstanceName>
    <StrengthNumber>137</StrengthNumber>
    <StrengthUnit>ug/1</StrengthUnit>
    <Pharm_Classes>l-Thyroxine [EPC],Thyroxine [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2021-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171012</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>68788-7026-9</NDCCode>
    <PackageDescription>90 TABLET in 1 BOTTLE (68788-7026-9) </PackageDescription>
    <NDC11Code>68788-7026-09</NDC11Code>
    <ProductNDC>68788-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Levothyroxine Sodium</ProprietaryName>
    <NonProprietaryName>Levothyroxine Sodium</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20171012</StartMarketingDate>
    <MarketingCategoryName>NDA AUTHORIZED GENERIC</MarketingCategoryName>
    <ApplicationNumber>NDA021342</ApplicationNumber>
    <LabelerName>Preferrred Pharmaeuticals Inc.</LabelerName>
    <SubstanceName>LEVOTHYROXINE SODIUM</SubstanceName>
    <StrengthNumber>137</StrengthNumber>
    <StrengthUnit>ug/1</StrengthUnit>
    <Pharm_Classes>l-Thyroxine [EPC],Thyroxine [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2021-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20201231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20171012</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>71872-7026-1</NDCCode>
    <PackageDescription>1 VIAL, MULTI-DOSE in 1 BAG (71872-7026-1)  &gt; 10 mL in 1 VIAL, MULTI-DOSE</PackageDescription>
    <NDC11Code>71872-7026-01</NDC11Code>
    <ProductNDC>71872-7026</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Quelicin</ProprietaryName>
    <NonProprietaryName>Succinylcholine Chloride</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <RouteName>INTRAMUSCULAR; INTRAVENOUS</RouteName>
    <StartMarketingDate>20140331</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA008845</ApplicationNumber>
    <LabelerName>Medical Purchasing Solutions, LLC</LabelerName>
    <SubstanceName>SUCCINYLCHOLINE CHLORIDE</SubstanceName>
    <StrengthNumber>20</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2025-01-01</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180228</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Succinylcholine chloride is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.</IndicationAndUsage>
    <Description>Quelicin (Succinylcholine Chloride Injection, USP) is a sterile, nonpyrogenic solution to be used as a short-acting, depolarizing, skeletal muscle relaxant. See HOW SUPPLIED for summary of content and characteristics of the solutions. The solutions are for I.M. or I.V. use. Succinylcholine Chloride, USP is chemically designated C 14H 30Cl 2N 2O 4 and its molecular weight is 361.31. It has the following structural formula. Succinylcholine is a diquaternary base consisting of the dichloride salt of the dicholine ester of succinic acid. It is a white, odorless, slightly bitter powder, very soluble in water. The drug is incompatible with alkaline solutions but relatively stable in acid solutions. Solutions of the drug lose potency unless refrigerated. Solution intended for multiple-dose administration contains 0.18% methylparaben and 0.02% propylparaben as preservatives (List No. 6629). Product not requiring dilution (multiple-dose fliptop vial) contains sodium chloride to render isotonic. May contain sodium hydroxide and/or hydrochloric acid for pH adjustment. pH is 3.6 (3.0 to 4.5). See table in HOW SUPPLIED for characteristics. Sodium Chloride, USP, chemically designated NaCl, is a white crystalline compound freely soluble in water.</Description>
  </NDC>
  <NDC>
    <NDCCode>50114-0104-6</NDCCode>
    <PackageDescription>10 AMPULE in 1 CARTON (50114-0104-6)  &gt; 2.2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>50114-0104-06</NDC11Code>
    <ProductNDC>50114-0104</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Tonsilla Compositum</ProprietaryName>
    <NonProprietaryName>Conium Maculatum Flowering Top, Solanum Dulcamara Top, Echinacea, Unspecified, Horse Chestnut,antimony Potassium Tartrate, Ascorbic Acid, Protortonia Cacti,galium Aparine,gentiana Lutea Root,geranium Robertianum, Pulsatilla Vulgaris,lactic Acid, L-, Sus Scrofa Adrenal Gland,sulfur,tribasic Calcium Phosphate,ferrosoferric Phosphate,sus Scrofa Umbilical Cord,pork Liver,sus Scrofa Hypothalamussus Scrofa Bone Marrow,sus Scrofa Spleen,sus Scrofa Adrenal Gland, Cortisone Acetate, Sus Scrofa Embryo,</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>CONIUM MACULATUM FLOWERING TOP; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; HORSE CHESTNUT; ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; PROTORTONIA CACTI; GALIUM APARINE; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; PULSATILLA VULGARIS; LACTIC ACID, L-; SULFUR; TRIBASIC CALCIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; SUS SCROFA ADRENAL GLAND; CORTISONE ACETATE; SUS SCROFA EMBRYO; MERCURIUS SOLUBILIS; LEVOTHYROXINE; BARIUM CARBONATE; SUS SCROFA TONSIL</SubstanceName>
    <StrengthNumber>4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 10; 10; 10; 10; 10; 10; 10; 13; 13; 13; 13; 13; 28; 28</StrengthNumber>
    <StrengthUnit>[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; 1/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL</StrengthUnit>
    <Pharm_Classes>Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2017-01-30</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0110-6</NDCCode>
    <PackageDescription>10 VIAL in 1 CARTON (50114-0110-6)  &gt; 2.2 mL in 1 VIAL</PackageDescription>
    <NDC11Code>50114-0110-06</NDC11Code>
    <ProductNDC>50114-0110</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Solidago Compositum</ProprietaryName>
    <NonProprietaryName>Solidago Virgaurea Flowering Top And Baptisia Tinctoria Root And Berberis Vulgaris Root Bark And Equisetum Hyemale And Silver Nitrate And Lytta Vesicatoria And Capsicum And Cupric Sulfate And Clerodendranthus Spicatus Leaf And Chondrodendron Tomentosum Root And Smilax Regelii Root And Turpentine Oil And Apis Mellifera Venom And Agathosma Betulina Leaf And Human Coxsackievirus A And Mercuric Chloride And Sus Scrofa Urinary Bladder And Calcium Sulfide And Sodium Pyruvate</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>SOLIDAGO VIRGAUREA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; EQUISETUM HYEMALE; SILVER NITRATE; LYTTA VESICATORIA; CAPSICUM; CUPRIC SULFATE; CLERODENDRANTHUS SPICATUS LEAF; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX REGELII ROOT; TURPENTINE OIL; APIS MELLIFERA VENOM; AGATHOSMA BETULINA LEAF; HUMAN COXSACKIEVIRUS A; MERCURIC CHLORIDE; SUS SCROFA URINARY BLADDER; CALCIUM SULFIDE; SODIUM PYRUVATE; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; ESCHERICHIA COLI; ARSENIC TRIOXIDE</SubstanceName>
    <StrengthNumber>3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 13; 28</StrengthNumber>
    <StrengthUnit>[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>50114-0113-6</NDCCode>
    <PackageDescription>10 AMPULE in 1 CARTON (50114-0113-6)  &gt; 2.2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>50114-0113-06</NDC11Code>
    <ProductNDC>50114-0113</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Echinacea Compositum Forte</ProprietaryName>
    <NonProprietaryName>Aconitum Napellus,echinacea, Unspecified, Arnica Montana Root, Baptisia Tinctoria Root ,toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Euphorbia Resinifera Resin, Gelsemium Sempervirens Root, Phytolacca Americana Root, Silver Nitrate, Arsenic Trioxide, Mercuric Chloride, Phosphorus, Pulsatilla Vulgaris, Sulfur,thuja Occidentalis Leafy Twig,calcium Sulfide,lachesis Muta Venom,</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; ARNICA MONTANA ROOT; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CORTISONE ACETATE; ECHINACEA, UNSPECIFIED; EUPATORIUM PERFOLIATUM FLOWERING TOP; EUPHORBIA RESINIFERA RESIN; GELSEMIUM SEMPERVIRENS ROOT; INFLUENZA A VIRUS; LACHESIS MUTA VENOM; MERCURIC CHLORIDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; SANGUINARIA CANADENSIS ROOT; SILVER NITRATE; STAPHYLOCOCCUS EPIDERMIDIS; STAPHYLOCOCCUS HAEMOLYTICUS; STAPHYLOCOCCUS SIMULANS; STREPTOCOCCUS PYOGENES; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON PUBESCENS LEAF; ZINC</SubstanceName>
    <StrengthNumber>5; 6; 10; 6; 8; 12; 15; 3; 8; 8; 8; 15; 12; 8; 10; 8; 10; 6; 10; 20; 20; 20; 20; 10; 10; 6; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL</StrengthUnit>
    <Pharm_Classes>Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2014-08-22</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0114-2</NDCCode>
    <PackageDescription>10 VIAL, SINGLE-DOSE in 1 CARTON (50114-0114-2)  &gt; .45 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>50114-0114-02</NDC11Code>
    <ProductNDC>50114-0114</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Oculoheel</ProprietaryName>
    <NonProprietaryName>Cochlearia Officinalis Flowering Top,echinacea Angustifolia,euphrasia Stricta And Pilocarpus Jaborandi Leaf</NonProprietaryName>
    <DosageFormName>SOLUTION/ DROPS</DosageFormName>
    <RouteName>INTRAOCULAR</RouteName>
    <StartMarketingDate>20050627</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>COCHLEARIA OFFICINALIS FLOWERING TOP; ECHINACEA, UNSPECIFIED; EUPHRASIA STRICTA; PILOCARPUS JABORANDI LEAF</SubstanceName>
    <StrengthNumber>5; 5; 5; 5</StrengthNumber>
    <StrengthUnit>[hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2017-01-30</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0119-2</NDCCode>
    <PackageDescription>15 VIAL, SINGLE-DOSE in 1 CARTON (50114-0119-2)  &gt; .45 mL in 1 VIAL, SINGLE-DOSE</PackageDescription>
    <NDC11Code>50114-0119-02</NDC11Code>
    <ProductNDC>50114-0119</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Clearlife</ProprietaryName>
    <NonProprietaryName>Cochlearia Officinalis Flowering Top, Echinacea, Unspecified, Euphrasia Stricta And Pilocarpus Jaborandi Leaf</NonProprietaryName>
    <DosageFormName>SOLUTION/ DROPS</DosageFormName>
    <RouteName>OPHTHALMIC</RouteName>
    <StartMarketingDate>20130404</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>COCHLEARIA OFFICINALIS FLOWERING TOP; ECHINACEA, UNSPECIFIED; EUPHRASIA STRICTA; PILOCARPUS JABORANDI LEAF</SubstanceName>
    <StrengthNumber>5; 5; 5; 5</StrengthNumber>
    <StrengthUnit>[hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL; [hp_X]/.45mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-08-29</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0150-9</NDCCode>
    <PackageDescription>1 BOTTLE, PUMP in 1 CARTON (50114-0150-9)  &gt; 20 mL in 1 BOTTLE, PUMP</PackageDescription>
    <NDC11Code>50114-0150-09</NDC11Code>
    <ProductNDC>50114-0150</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Luffeel</ProprietaryName>
    <NonProprietaryName>Galphimia Glauca Flowering Top And Histamine Dihydrochloride And Luffa Operculata Fruit And Sulfur</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>NASAL</RouteName>
    <StartMarketingDate>20110705</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR</SubstanceName>
    <StrengthNumber>4; 12; 4; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2017-02-03</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0152-9</NDCCode>
    <PackageDescription>1 BOTTLE, PUMP in 1 CARTON (50114-0152-9)  &gt; 20 mL in 1 BOTTLE, PUMP</PackageDescription>
    <NDC11Code>50114-0152-09</NDC11Code>
    <ProductNDC>50114-0152</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Clearlife</ProprietaryName>
    <NonProprietaryName>Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit And Sulfur</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>NASAL</RouteName>
    <StartMarketingDate>20130411</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; LUFFA OPERCULATA FRUIT; SULFUR</SubstanceName>
    <StrengthNumber>4; 12; 4; 12</StrengthNumber>
    <StrengthUnit>[hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL; [hp_X]/20mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-08-29</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0227-2</NDCCode>
    <PackageDescription>30000 mg in 1 BOTTLE (50114-0227-2)</PackageDescription>
    <NDC11Code>50114-0227-02</NDC11Code>
    <ProductNDC>50114-0227</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Atropinum Compositum Rx</ProprietaryName>
    <NonProprietaryName>Atropine Sulfate And Bryonia Alba Root And Arsenic Trioxide And Berberis Vulgaris Root Bark And Citrullus Colocynthis Fruit Pulp And Cupric Acetate And Chondrodendron Tomentosum Root And Veratrum Album Root And Baptisia Tinctoria Root And Chelidonium Majus And Lytta Vesicatoria And Gonorrheal Urethral Secretion Human And Clematis Recta Flowering Top And Thuja Occidentalis Leafy Twig And Benzoic Acid And Silver Nitrate</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20030830</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>ATROPINE SULFATE; BRYONIA ALBA ROOT; ARSENIC TRIOXIDE; BERBERIS VULGARIS ROOT BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; CHONDRODENDRON TOMENTOSUM ROOT; VERATRUM ALBUM ROOT; BAPTISIA TINCTORIA ROOT; CHELIDONIUM MAJUS; LYTTA VESICATORIA; GONORRHEAL URETHRAL SECRETION HUMAN; CLEMATIS RECTA FLOWERING TOP; THUJA OCCIDENTALIS LEAFY TWIG; BENZOIC ACID; SILVER NITRATE</SubstanceName>
    <StrengthNumber>4; 1; 4; 1; 1; 2; 1; 1; 1; 1; 5; 10; 1; 1; 2; 1</StrengthNumber>
    <StrengthUnit>[hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg</StrengthUnit>
    <Pharm_Classes>Ammonium Ion Binding Activity [MoA],Nitrogen Binding Agent [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2017-04-04</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-0988-4</NDCCode>
    <PackageDescription>50 mL in 1 BOTTLE (50114-0988-4)</PackageDescription>
    <NDC11Code>50114-0988-04</NDC11Code>
    <ProductNDC>50114-0988</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Anacardium Homaccord</ProprietaryName>
    <NonProprietaryName>Semecarpus Anacardium Juice And Iodine And Ipecac</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19860131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>SEMECARPUS ANACARDIUM JUICE; IODINE; IPECAC</SubstanceName>
    <StrengthNumber>6; 30; 4</StrengthNumber>
    <StrengthUnit>[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2017-02-24</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-1000-4</NDCCode>
    <PackageDescription>50 mL in 1 BOTTLE (50114-1000-4)</PackageDescription>
    <NDC11Code>50114-1000-04</NDC11Code>
    <ProductNDC>50114-1000</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Aesculus Compositum</ProprietaryName>
    <NonProprietaryName>Horse Chestnut And Echinacea Pallida And Arnica Montana Root And Claviceps Purpurea Sclerotium And Viscum Album Whole And Apis Mellifera And Baptisia Tinctoria Root And Benzoic Acid And Colchicum Autu</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19860131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>APIS MELLIFERA; ARNICA MONTANA ROOT; BAPTISIA TINCTORIA ROOT; BARIUM IODIDE; BENZOIC ACID; CLAVICEPS PURPUREA SCLEROTIUM; COLCHICUM AUTUMNALE BULB; COPPER; ECHINACEA PALLIDA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HORSE CHESTNUT; LEAD IODIDE; RUTA GRAVEOLENS FLOWERING TOP; SOLANUM DULCAMARA STEM; SOLANUM NIGRUM WHOLE; TOBACCO LEAF; TOXICODENDRON PUBESCENS LEAF; VISCUM ALBUM WHOLE</SubstanceName>
    <StrengthNumber>4; 3; 4; 6; 4; 3; 4; 13; 2; 4; 1; 20; 4; 4; 6; 10; 4; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-08-29</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-1010-4</NDCCode>
    <PackageDescription>50 mL in 1 BOTTLE (50114-1010-4)</PackageDescription>
    <NDC11Code>50114-1010-04</NDC11Code>
    <ProductNDC>50114-1010</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Arnica-heel</ProprietaryName>
    <NonProprietaryName>Apis Mellifera And Baptisia Tinctoria Root And Solanum Dulcamara Stem And Eucalyptus Globulus Leaf And Solanum Nigrum Whole And Toxicodendron Pubescens Leaf And Eupatorium Cannabinum And Arnica Montan</NonProprietaryName>
    <DosageFormName>LIQUID</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19860131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>APIS MELLIFERA; ARNICA MONTANA ROOT; BAPTISIA TINCTORIA ROOT; BENZOIC ACID; BRYONIA ALBA ROOT; COLCHICUM AUTUMNALE BULB; ECHINACEA, UNSPECIFIED; EUCALYPTUS GLOBULUS LEAF; EUPATORIUM CANNABINUM; MERCURIALIS PERENNIS; SOLANUM DULCAMARA STEM; SOLANUM LYCOPERSICUM; SOLANUM NIGRUM WHOLE; TOXICODENDRON PUBESCENS LEAF</SubstanceName>
    <StrengthNumber>4; 3; 4; 3; 4; 4; 3; 4; 2; 3; 4; 3; 4; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-11-21</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-1032-6</NDCCode>
    <PackageDescription>10 VIAL in 1 CARTON (50114-1032-6)  &gt; 1.1 mL in 1 VIAL</PackageDescription>
    <NDC11Code>50114-1032-06</NDC11Code>
    <ProductNDC>50114-1032</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Cimicifuga-homaccord</ProprietaryName>
    <NonProprietaryName>Black Cohosh And Strontium Carbonate</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>BLACK COHOSH; STRONTIUM CARBONATE</SubstanceName>
    <StrengthNumber>4; 8</StrengthNumber>
    <StrengthUnit>[hp_X]/1.1mL; [hp_X]/1.1mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-11-21</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-1034-6</NDCCode>
    <PackageDescription>10 VIAL in 1 CARTON (50114-1034-6)  &gt; 1.1 mL in 1 VIAL</PackageDescription>
    <NDC11Code>50114-1034-06</NDC11Code>
    <ProductNDC>50114-1034</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Colocynthis-homaccord</ProprietaryName>
    <NonProprietaryName>Citrullus Colocynthis Fruit Pulp And Pseudognaphalium Obtusifolium</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>CITRULLUS COLOCYNTHIS FRUIT PULP; PSEUDOGNAPHALIUM OBTUSIFOLIUM</SubstanceName>
    <StrengthNumber>4; 3</StrengthNumber>
    <StrengthUnit>[hp_X]/1.1mL; [hp_X]/1.1mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2015-06-26</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>50114-1058-6</NDCCode>
    <PackageDescription>10 AMPULE in 1 CARTON (50114-1058-6)  &gt; 2.2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>50114-1058-06</NDC11Code>
    <ProductNDC>50114-1058</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Cor Compositum</ProprietaryName>
    <NonProprietaryName>Selenicereus Grandiflorus Stem, Arnica Montana Root, Nitroglycerin,potassium Carbonate, Kalmia Latifolia Leaf, Crataegus Laevigata Fruit,strychnos Ignatii Seed, Ranunculus Bulbosus, Lactic Acid, L-,arsenic Trioxide, Pork Heart, Fumaric Acid, Pork Liver,.alpha.-ketoglutaric Acid, Malic Acid, Sodium Diethyl Oxalacetate, Ouabain, Naja Naja Venom,spigelia Anthelmia And Activated Charcoal</NonProprietaryName>
    <DosageFormName>SOLUTION</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>19930131</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Heel Inc</LabelerName>
    <SubstanceName>.ALPHA.-KETOGLUTARIC ACID; ACTIVATED CHARCOAL; ARNICA MONTANA ROOT; ARSENIC TRIOXIDE; CRATAEGUS LAEVIGATA FRUIT; FUMARIC ACID; KALMIA LATIFOLIA LEAF; LACTIC ACID, L-; MALIC ACID; NAJA NAJA VENOM; NITROGLYCERIN; OUABAIN; PORK HEART; PORK LIVER; POTASSIUM CARBONATE; RANUNCULUS BULBOSUS; SELENICEREUS GRANDIFLORUS STEM; SPIGELIA ANTHELMIA; STRYCHNOS IGNATII SEED</SubstanceName>
    <StrengthNumber>8; 18; 4; 8; 6; 8; 4; 6; 8; 10; 4; 8; 8; 8; 4; 6; 3; 10; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL</StrengthUnit>
    <Pharm_Classes>Nitrate Vasodilator [EPC],Nitrates [Chemical/Ingredient],Vasodilation [PE]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2014-08-22</LastUpdate>
  </NDC>
</NDCList>
                    

<NDCList><NDC><NDCCode>50114-7026-1</NDCCode><ProprietaryName>Lymphomyosot</ProprietaryName><NonProprietaryName>Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine</NonProprietaryName></NDC><NDC><NDCCode>50114-7026-2</NDCCode><ProprietaryName>Lymphomyosot</ProprietaryName><NonProprietaryName>Geranium Robertianum, Nasturtium Officinale, Ferrous Iodide, Juglans Regia Leaf, Juglans Regia Fruit Rind, Immature, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Veronica Officinalis Flowering Top, Equisetum Hyemale, Fumaria Officinalis Flowering Top, Sodium Sulfate, Pinus Sylvestris Flowering Top,gentiana Lutea Root, Araneus Diadematus, Smilax Regelii Root, Tribasic Calcium Phosphate And Levothyroxine</NonProprietaryName></NDC><NDC><NDCCode>0002-7026-60</NDCCode><ProprietaryName>Jaypirca</ProprietaryName><NonProprietaryName>Pirtobrutinib</NonProprietaryName></NDC><NDC><NDCCode>0002-7026-99</NDCCode><ProprietaryName>Jaypirca</ProprietaryName><NonProprietaryName>Pirtobrutinib</NonProprietaryName></NDC><NDC><NDCCode>0338-7026-06</NDCCode><ProprietaryName>Clinimix E</ProprietaryName><NonProprietaryName>Leucine, Phenylalanine, Lysine, Methionine, Isoleucine, Valine, Histidine, Threonine, Tryptophan, Alanine, Glycine, Arginine, Proline, Serine, Tyrosine, Sodium Acetate, Dibasic Potassium Phosphate, Magnesium Chloride, Sodium Chloride, Calcium Chloride, Dextrose</NonProprietaryName></NDC><NDC><NDCCode>0440-7026-30</NDCCode><ProprietaryName>Acetaminophen And Codeine</ProprietaryName><NonProprietaryName>Acetaminophen And Codeine Phosphate</NonProprietaryName></NDC><NDC><NDCCode>0440-7026-40</NDCCode><ProprietaryName>Acetaminophen And Codeine</ProprietaryName><NonProprietaryName>Acetaminophen And Codeine Phosphate</NonProprietaryName></NDC><NDC><NDCCode>0904-7026-61</NDCCode><ProprietaryName>Nitrofurantoin Macrocrystals</ProprietaryName><NonProprietaryName>Nitrofurantoin Macrocrystals</NonProprietaryName></NDC><NDC><NDCCode>10888-7026-1</NDCCode><NonProprietaryName>Docusate Sodium</NonProprietaryName></NDC><NDC><NDCCode>50090-7026-1</NDCCode><ProprietaryName>Cephalexin</ProprietaryName><NonProprietaryName>Cephalexin</NonProprietaryName></NDC><NDC><NDCCode>50090-7026-3</NDCCode><ProprietaryName>Cephalexin</ProprietaryName><NonProprietaryName>Cephalexin</NonProprietaryName></NDC><NDC><NDCCode>52731-7026-2</NDCCode><ProprietaryName>Air Pollution Complex</ProprietaryName><NonProprietaryName>Arnica Montana 6x, Bovista 6x, Calcarea Carbonica 8x,carbo Vegetabilis 8x, Cicuta Virosa 6x, Euphorbium Officinarum 6x,hydrastis Canadensis 4x, Petroleum 6x, Phosphorus 8x, Plumbum Metallicum 8x, Sulf</NonProprietaryName></NDC><NDC><NDCCode>62670-7026-0</NDCCode><ProprietaryName>Anti Bacterial Hand Gel</ProprietaryName><NonProprietaryName>Alcohol</NonProprietaryName></NDC><NDC><NDCCode>68788-7026-3</NDCCode><ProprietaryName>Levothyroxine Sodium</ProprietaryName><NonProprietaryName>Levothyroxine Sodium</NonProprietaryName></NDC><NDC><NDCCode>68788-7026-9</NDCCode><ProprietaryName>Levothyroxine Sodium</ProprietaryName><NonProprietaryName>Levothyroxine Sodium</NonProprietaryName></NDC><NDC><NDCCode>71872-7026-1</NDCCode><ProprietaryName>Quelicin</ProprietaryName><NonProprietaryName>Succinylcholine Chloride</NonProprietaryName></NDC><NDC><NDCCode>50114-0104-6</NDCCode><ProprietaryName>Tonsilla Compositum</ProprietaryName><NonProprietaryName>Conium Maculatum Flowering Top, Solanum Dulcamara Top, Echinacea, Unspecified, Horse Chestnut,antimony Potassium Tartrate, Ascorbic Acid, Protortonia Cacti,galium Aparine,gentiana Lutea Root,geranium Robertianum, Pulsatilla Vulgaris,lactic Acid, L-, Sus Scrofa Adrenal Gland,sulfur,tribasic Calcium Phosphate,ferrosoferric Phosphate,sus Scrofa Umbilical Cord,pork Liver,sus Scrofa Hypothalamussus Scrofa Bone Marrow,sus Scrofa Spleen,sus Scrofa Adrenal Gland, Cortisone Acetate, Sus Scrofa Embryo,</NonProprietaryName></NDC><NDC><NDCCode>50114-0110-6</NDCCode><ProprietaryName>Solidago Compositum</ProprietaryName><NonProprietaryName>Solidago Virgaurea Flowering Top And Baptisia Tinctoria Root And Berberis Vulgaris Root Bark And Equisetum Hyemale And Silver Nitrate And Lytta Vesicatoria And Capsicum And Cupric Sulfate And Clerodendranthus Spicatus Leaf And Chondrodendron Tomentosum Root And Smilax Regelii Root And Turpentine Oil And Apis Mellifera Venom And Agathosma Betulina Leaf And Human Coxsackievirus A And Mercuric Chloride And Sus Scrofa Urinary Bladder And Calcium Sulfide And Sodium Pyruvate</NonProprietaryName></NDC><NDC><NDCCode>50114-0113-6</NDCCode><ProprietaryName>Echinacea Compositum Forte</ProprietaryName><NonProprietaryName>Aconitum Napellus,echinacea, Unspecified, Arnica Montana Root, Baptisia Tinctoria Root ,toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Bryonia Alba Root, Eupatorium Perfoliatum Flowering Top, Euphorbia Resinifera Resin, Gelsemium Sempervirens Root, Phytolacca Americana Root, Silver Nitrate, Arsenic Trioxide, Mercuric Chloride, Phosphorus, Pulsatilla Vulgaris, Sulfur,thuja Occidentalis Leafy Twig,calcium Sulfide,lachesis Muta Venom,</NonProprietaryName></NDC><NDC><NDCCode>50114-0114-2</NDCCode><ProprietaryName>Oculoheel</ProprietaryName><NonProprietaryName>Cochlearia Officinalis Flowering Top,echinacea Angustifolia,euphrasia Stricta And Pilocarpus Jaborandi Leaf</NonProprietaryName></NDC><NDC><NDCCode>50114-0119-2</NDCCode><ProprietaryName>Clearlife</ProprietaryName><NonProprietaryName>Cochlearia Officinalis Flowering Top, Echinacea, Unspecified, Euphrasia Stricta And Pilocarpus Jaborandi Leaf</NonProprietaryName></NDC><NDC><NDCCode>50114-0150-9</NDCCode><ProprietaryName>Luffeel</ProprietaryName><NonProprietaryName>Galphimia Glauca Flowering Top And Histamine Dihydrochloride And Luffa Operculata Fruit And Sulfur</NonProprietaryName></NDC><NDC><NDCCode>50114-0152-9</NDCCode><ProprietaryName>Clearlife</ProprietaryName><NonProprietaryName>Galphimia Glauca Flowering Top, Histamine Dihydrochloride, Luffa Operculata Fruit And Sulfur</NonProprietaryName></NDC><NDC><NDCCode>50114-0227-2</NDCCode><ProprietaryName>Atropinum Compositum Rx</ProprietaryName><NonProprietaryName>Atropine Sulfate And Bryonia Alba Root And Arsenic Trioxide And Berberis Vulgaris Root Bark And Citrullus Colocynthis Fruit Pulp And Cupric Acetate And Chondrodendron Tomentosum Root And Veratrum Album Root And Baptisia Tinctoria Root And Chelidonium Majus And Lytta Vesicatoria And Gonorrheal Urethral Secretion Human And Clematis Recta Flowering Top And Thuja Occidentalis Leafy Twig And Benzoic Acid And Silver Nitrate</NonProprietaryName></NDC><NDC><NDCCode>50114-0988-4</NDCCode><ProprietaryName>Anacardium Homaccord</ProprietaryName><NonProprietaryName>Semecarpus Anacardium Juice And Iodine And Ipecac</NonProprietaryName></NDC><NDC><NDCCode>50114-1000-4</NDCCode><ProprietaryName>Aesculus Compositum</ProprietaryName><NonProprietaryName>Horse Chestnut And Echinacea Pallida And Arnica Montana Root And Claviceps Purpurea Sclerotium And Viscum Album Whole And Apis Mellifera And Baptisia Tinctoria Root And Benzoic Acid And Colchicum Autu</NonProprietaryName></NDC><NDC><NDCCode>50114-1010-4</NDCCode><ProprietaryName>Arnica-heel</ProprietaryName><NonProprietaryName>Apis Mellifera And Baptisia Tinctoria Root And Solanum Dulcamara Stem And Eucalyptus Globulus Leaf And Solanum Nigrum Whole And Toxicodendron Pubescens Leaf And Eupatorium Cannabinum And Arnica Montan</NonProprietaryName></NDC><NDC><NDCCode>50114-1032-6</NDCCode><ProprietaryName>Cimicifuga-homaccord</ProprietaryName><NonProprietaryName>Black Cohosh And Strontium Carbonate</NonProprietaryName></NDC><NDC><NDCCode>50114-1034-6</NDCCode><ProprietaryName>Colocynthis-homaccord</ProprietaryName><NonProprietaryName>Citrullus Colocynthis Fruit Pulp And Pseudognaphalium Obtusifolium</NonProprietaryName></NDC><NDC><NDCCode>50114-1058-6</NDCCode><ProprietaryName>Cor Compositum</ProprietaryName><NonProprietaryName>Selenicereus Grandiflorus Stem, Arnica Montana Root, Nitroglycerin,potassium Carbonate, Kalmia Latifolia Leaf, Crataegus Laevigata Fruit,strychnos Ignatii Seed, Ranunculus Bulbosus, Lactic Acid, L-,arsenic Trioxide, Pork Heart, Fumaric Acid, Pork Liver,.alpha.-ketoglutaric Acid, Malic Acid, Sodium Diethyl Oxalacetate, Ouabain, Naja Naja Venom,spigelia Anthelmia And Activated Charcoal</NonProprietaryName></NDC></NDCList>
                    

Using REST to Invoke DataLabs API

Introduction

This document is intended for developers who want to write applications that can interact with the DataLabs REST API. With DataLabs Web Services, you can create a customized services for your own website or application. You can use the REST API to retrieve DataLabs Web Services results programmatically.

Important: The REST API requires the use of an API key, which you can get from the DataLabs MyAccount Console.

Working With DataLabs REST API

You can retrieve results for a particular operation (search, getcode, etc) by sending an HTTP GET request to its URI.
For instance, the URI for a “search” request has the following format:

https://www.datalabs.health/api/{domain}/{operation}?q={query}&rt={result type}&token={token}

If the request succeeds, the server responds with a 200 OK HTTP status code and the response data.

Four parameters are required with each “search” request:

• Use the domain parameter to specify required data domain.
• Use the operation parameter to specify “format_check” operation.
• Use the q (query) parameter to specify your query.
• Use the token (API key) query parameter to identify your application.

Optional parameter:

• Use the rt (result type) parameter to specify required result type (json/xml/min.json/min.xml).

All other query parameters (if any) are optional.

Full list of API parameters:

• Use the domain parameter to specify required data domain.
• Use the operation parameter to specify “format_check” operation.
• Use the q (query) parameter to specify your query.
• Use the token (API key) query parameter to identify your application.
• Use the tin (tin number) parameter to specify your query about tin number.
• Use the tinname (tin name) parameter to specify your query about tin name.
• Use the zipcode (zip code) parameter to specify your query about zip code.
• Use the radius (radius) parameter to specify your query about radius.
• Use the fromdate (fromdate) parameter to specify your query about from date.
• Use the todate (todate) parameter to specify your query about to date.

Operations Currently Available in the DataLabs REST API

Currently DataLabs RESTful Lookup Service supports following operations:

• check_status — this method allows to get current code status.
• getcode — this method allows retrieval of full infrormation regarding one item based on the provided key.
• getcodes — this method allows retrieval of full infrormation regarding number of items based on the provided keys (q=1285636522,1730198755,1427145176,1487730636).
• search — allows retrieval of set of items based on the free-form lookup query.
• search_and_keywords — returns not only free-form lookup results but also keywords relevant to the original query.

Plus there are three NPI-specific operations:

• validate — allows to determine whether provider's information is valid based on data in the CMS database.
• paginate_with_predicates — provides server side data pagination using sorting and ordering criteria.
• search_with_predicates — this method is a "blend" of free text search and traditional prdeicate-based data selection.
• zipradius — allows to get npis by zipcode & radius.
• npideactivated — allows to get deactivated npis between two dates.

REST Search Examples

Query Parameter Reference

The query parameters you can use with the DataLabs REST API are summarized in the following table.
All parameter values need to be URL encoded.

Use Case #1 - I Need to Find Healthcare Provider (Doctor or Orgranization) Having Just Partial Information

So, you have to find healthcare provider having just partial information. For instance all you have is "EYE doctor RANIA in REDMOND". Strictly speaking, it is necessary to perform a search with minimum information and the maximum level of relevance of the result.

Coding example below demonstrates simplest implementation in C# language. By default DataLabs full text search API returns 30 results and, as you may see below, the first result in the list is "REDMOND EYE DOCTORS, PLLC" where dr. Rania Montecillo specified an owner.

Feel free to use and modify this code to find doctors you may know. If you provide more or less meaningfull information you will be pleasantly surprised to see them in the search results.

            
//--------------------------------------------------------------------------------------
// Fulltext search on NPI registry. Perform "search" operation to get most relevant results.
//--------------------------------------------------------------------------------------
using System;
using System.Net.Http;
using System.Threading.Tasks;

public class Program
{
    private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

    static async Task Main(string[] args)
    {
        string endPoint = $"https://www.datalabs.health/api/npi/search?q=EYE%20RANIA%20REDMOND&token={token}";
        using HttpClient client = new HttpClient();
        string response = await client.GetStringAsync(endPoint);

        Console.WriteLine(response);

        Console.WriteLine("Done. Press any key to exit ...");
        Console.ReadKey();
    }
}
            
        

            
{
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      "TaxonomyCode1": "207RI0200X",
      "Taxonomy1": "Infectious Disease",
      "LicenseNumber1": "39215",
      "LicenseNumberStateCode1": "KY",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "207RI0200X",
      "Taxonomy2": "Infectious Disease",
      "LicenseNumber2": "25MA07672000",
      "LicenseNumberStateCode2": "NJ",
      "PrimaryTaxonomySwitch2": "Y"
    },
    {
      "NPI": "1184645301",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "BAIK",
      "FirstName": "RANIA",
      "Credential": "D.O.",
      "FirstLineMailingAddress": "602 ROUTE 169",
      "SecondLineMailingAddress": "PO BOX 865",
      "MailingAddressCityName": "WOODSTOCK",
      "MailingAddressStateName": "CT",
      "MailingAddressPostalCode": "06281-2225",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "860-821-3406",
      "MailingAddressFaxNumber": "860-821-3407",
      "FirstLinePracticeLocationAddress": "602 ROUTE 169",
      "PracticeLocationAddressCityName": "WOODSTOCK",
      "PracticeLocationAddressStateName": "CT",
      "PracticeLocationAddressPostalCode": "06281-2225",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "860-821-3406",
      "PracticeLocationAddressFaxNumber": "860-821-3407",
      "EnumerationDate": "07/22/2006",
      "LastUpdateDate": "01/14/2016",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207Q00000X",
      "Taxonomy1": "Family Medicine",
      "LicenseNumber1": "000260",
      "LicenseNumberStateCode1": "CT",
      "PrimaryTaxonomySwitch1": "Y"
    },
    {
      "NPI": "1265443618",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "LOUTFI",
      "FirstName": "RANIA",
      "MiddleName": "H",
      "Credential": "MD",
      "FirstLineMailingAddress": "1 COOPER PLZ",
      "SecondLineMailingAddress": "THE COOPER HOSPITALIST TEAM",
      "MailingAddressCityName": "CAMDEN",
      "MailingAddressStateName": "NJ",
      "MailingAddressPostalCode": "08103-1461",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "856-342-3150",
      "MailingAddressFaxNumber": "856-968-8418",
      "FirstLinePracticeLocationAddress": "1 COOPER PLZ",
      "SecondLinePracticeLocationAddress": "THE COOPER HOSPITALIST TEAM",
      "PracticeLocationAddressCityName": "CAMDEN",
      "PracticeLocationAddressStateName": "NJ",
      "PracticeLocationAddressPostalCode": "08103-1461",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "856-342-3150",
      "PracticeLocationAddressFaxNumber": "856-968-8418",
      "EnumerationDate": "08/11/2006",
      "LastUpdateDate": "06/30/2014",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "207R00000X",
      "Taxonomy1": "Internal Medicine",
      "LicenseNumber1": "MA080819",
      "LicenseNumberStateCode1": "NJ",
      "PrimaryTaxonomySwitch1": "Y",
      "OtherIdentifier1": "01007800000",
      "OtherIdentifierType1": "OTHER",
      "OtherIdentifierIssuer1": "AMERICHOICE",
      "OtherIdentifier2": "0118460",
      "OtherIdentifierType2": "MEDICAID",
      "OtherIdentifierState2": "NJ",
      "OtherIdentifier3": "P00381177",
      "OtherIdentifierType3": "OTHER",
      "OtherIdentifierIssuer3": "RAIL ROAD MEDICARE",
      "OtherIdentifier4": "2798670000",
      "OtherIdentifierType4": "OTHER",
      "OtherIdentifierIssuer4": "AMERIHEALTH, HMO, KEYSTONE, IBC",
      "OtherIdentifier5": "1376273",
      "OtherIdentifierType5": "OTHER",
      "OtherIdentifierIssuer5": "AETNA US-HEALTHCARE",
      "OtherIdentifier6": "44132",
      "OtherIdentifierType6": "OTHER",
      "OtherIdentifierIssuer6": "UNIVERSITY HEALTH PLAN",
      "OtherIdentifier7": "60027465",
      "OtherIdentifierType7": "OTHER",
      "OtherIdentifierIssuer7": "HORIZON NJ HEALTH",
      "OtherIdentifier8": "3K6229",
      "OtherIdentifierType8": "OTHER",
      "OtherIdentifierIssuer8": "HEALTHNET",
      "OtherIdentifier9": "6761897",
      "OtherIdentifierType9": "OTHER",
      "OtherIdentifierIssuer9": "CIGNA"
    }
  ]
}

Done. Press any key to exit ...
            
        

Use Case #2 - I Need to Find Detailed Healthcare Provider Information Using Known NPI Number

This is very common scenario. You need to get full replica of NPI record. Again, it simple. Just use code provided below. API response may contain single NPI record, or empty list in case NPI does not exist in the CMS National Plan and Provider Enumeration System (NPPES) Registry.

                
    //--------------------------------------------------------------------------------------
    // Perform "getcode" operation to get healthcare provider information using NPI number.
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/getcode?q=1285636522&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "NPI": [
        {
          "NPI": "1285636522",
          "EntityType": "Organization",
          "EIN": "N/A",
          "IsOrgSubpart": "N",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER, INC",
          "FirstLineMailingAddress": "PO BOX 418283",
          "MailingAddressCityName": "BOSTON",
          "MailingAddressStateName": "MA",
          "MailingAddressPostalCode": "02241-8283",
          "MailingAddressCountryCode": "US",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400",
          "EnumerationDate": "06/01/2005",
          "LastUpdateDate": "11/25/2011",
          "AuthorizedOfficialLastName": "SCHNEIDER",
          "AuthorizedOfficialFirstName": "STEPHANIE",
          "AuthorizedOfficialTitle": "VP",
          "AuthorizedOfficialTelephoneNumber": "703-558-1403",
          "TaxonomyCode1": "207R00000X",
          "Taxonomy1": "Internal Medicine",
          "LicenseNumber1": "=========",
          "LicenseNumberStateCode1": "DC",
          "PrimaryTaxonomySwitch1": "Y",
          "OtherIdentifier1": "W677",
          "OtherIdentifierType1": "OTHER",
          "OtherIdentifierState1": "DC",
          "OtherIdentifierIssuer1": "BLUE SHIELD ADULT PCP GRP",
          "OtherIdentifier2": "027174100",
          "OtherIdentifierType2": "MEDICAID",
          "OtherIdentifierState2": "DC",
          "OtherIdentifier3": "097005100",
          "OtherIdentifierType3": "MEDICAID",
          "OtherIdentifierState3": "MD",
          "OtherIdentifier4": "442AGE",
          "OtherIdentifierType4": "OTHER",
          "OtherIdentifierState4": "MD",
          "OtherIdentifierIssuer4": "BLUE SHIELD PEDS PCP GRP#",
          "OtherIdentifier5": "6572",
          "OtherIdentifierType5": "OTHER",
          "OtherIdentifierState5": "DC",
          "OtherIdentifierIssuer5": "BLUE SHIELD GROUP NUMBER",
          "OtherIdentifier6": "W675",
          "OtherIdentifierType6": "OTHER",
          "OtherIdentifierState6": "DC",
          "OtherIdentifierIssuer6": "BLUE SHIELD PEDS PCP GRP#",
          "HealthcareProviderTaxonomyGroup1": "193200000X MULTI-SPECIALTY GROUP",
          "HealthcareProviderTaxonomyGroupDescription1": "Multi-Specialty Group - A business group of one or more individual practitioners, who practice with different areas of specialization."
        }
      ]
    }
    Done. Press any key to exit ...
                
            

Use Case #3 - I Need to Get Multiple Healthcare Providers Using List of NPI Numbers

You may need to perform bulk search for performance optimization. The "getcodes" operation allows you to decrease number of round trips in orders of magnitude. For instance you can get information about hundred NPI in one REST call, instead of sending NPI numbers one-by-one.

                
    //--------------------------------------------------------------------------------------
    // Perform "getcodes" operation to get multiple healthcare providers using list of NPIs. 
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/getcodes?q=1285636522,1730198755,1427145176&rt=minjson&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "NPI": [
        {
          "NPI": "1285636522",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER, INC",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400"
        },
        {
          "NPI": "1730198755",
          "OrgName": "MEDSTAR GEORGETOWN MEDICAL CENTER",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "888-896-1400"
        },
        {
          "NPI": "1427145176",
          "OrgName": "MEDSTAR - GEORGETOWN MEDICAL CENTER, INC.",
          "OtherOrgName": "GEORGETOWN UNIVERSITY HOSPITAL",
          "OtherOrgNameTypeCode": "3",
          "FirstLinePracticeLocationAddress": "3800 RESERVOIR RD., NW",
          "PracticeLocationAddressCityName": "WASHINGTON",
          "PracticeLocationAddressStateName": "DC",
          "PracticeLocationAddressPostalCode": "20007-2113",
          "PracticeLocationAddressCountryCode": "US",
          "PracticeLocationAddressTelephoneNumber": "202-444-3000",
          "PracticeLocationAddressFaxNumber": "202-444-3095"
        }
      ]
    }
    Done. Press any key to exit ...
                
            

Use Case #4 - I Need to Check NPI Number Status

Again, very common scenario. You just need to check NPI number status. It is simple. Take a look at the code below. Expected result contains requested NPI number, status, and short status description.

                
    //--------------------------------------------------------------------------------------
    // Perform "check_status" operation to get NPI Number status (active, deactivated, etc).
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/check_status?q=1285636522&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
    {
      "Code": "1285636522",
      "Status": "Active",
      "Message": "\"1285636522\" NPI Number does exist and has \"active\" status"
    }
                
    Done. Press any key to exit ...
                
            

Use Case #5 - I need to retrieve a list of healthcare providers based on specified search parameters.

The system allows users to retrieve a list of healthcare providers by filtering on specified fields (e.g., organization name, state, city, ZIP code, etc.). The example below demonstrates how to retrieve all providers with a specified city, state, and ZIP code.

                
    //--------------------------------------------------------------------------------------
    // Perform "search_with_predicates" operation to get multiple healthcare providers using specified city, state, and ZIP code. 
    //--------------------------------------------------------------------------------------
    using System;
    using System.Net.Http;
    using System.Threading.Tasks;

    public class Program
    {
        private const string token = "3932f3b0-cfab-11dc-95ff-0800200c9a663932f3b0-cfab-11dc-95ff-0800200c9a66";

        static async Task Main(string[] args)
        {
            string endPoint = $"https://www.datalabs.health/api/npi/search_with_predicates?q=&qf=City:true:REDMOND&qf=State:true:OR&qf=Zip:true:97756-9069&rt=json&token={token}";
            using HttpClient client = new HttpClient();
            string response = await client.GetStringAsync(endPoint);

            Console.WriteLine(response);

            Console.WriteLine("Done. Press any key to exit ...");
            Console.ReadKey();
        }
    }
                
            

                
{
  "NPI": [
    {
      "NPI": "1083349906",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "STAFFORD",
      "FirstName": "KADY",
      "NamePrefix": "MS.",
      "Credential": "LPC",
      "FirstLineMailingAddress": "13574 SW HIGHWAY 126",
      "MailingAddressCityName": "POWELL BUTTE",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97753-1541",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-480-6360",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-203-0307",
      "EnumerationDate": "07/24/2022",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YP2500X",
      "Taxonomy1": "Professional Counselor",
      "LicenseNumber1": "LPC6225",
      "LicenseNumberStateCode1": "ID",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C9084",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1215724679",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "SCHAY",
      "FirstName": "ANGELICA",
      "MiddleName": "NICOLE",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1841",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1841",
      "EnumerationDate": "04/21/2025",
      "LastUpdateDate": "04/21/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101Y00000X",
      "Taxonomy1": "Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/21/2025",
      "PrimaryTaxonomyCode": "101Y00000X",
      "PrimaryTaxonomy": "Counselor"
    },
    {
      "NPI": "1013556505",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "IVENS",
      "FirstName": "KRYSTA",
      "FirstLineMailingAddress": "743 NW QUINCE AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-1250",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "360-526-1448",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "971-217-6150",
      "EnumerationDate": "12/31/2019",
      "LastUpdateDate": "02/15/2025",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "N",
      "TaxonomyCode2": "101YP2500X",
      "Taxonomy2": "Professional Counselor",
      "LicenseNumber2": "C7963",
      "LicenseNumberStateCode2": "OR",
      "PrimaryTaxonomySwitch2": "Y",
      "CertificationDate": "02/15/2025",
      "PrimaryTaxonomyCode": "101YP2500X",
      "PrimaryTaxonomy": "Professional Counselor"
    },
    {
      "NPI": "1497336275",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "ARANT",
      "FirstName": "ERIN",
      "MiddleName": "HENNESSEY",
      "FirstLineMailingAddress": "4639 SW 37TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-6776",
      "MailingAddressCountryCode": "US",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "04/14/2021",
      "LastUpdateDate": "04/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "225X00000X",
      "Taxonomy1": "Occupational Therapist",
      "LicenseNumber1": "390047",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "04/14/2021",
      "PrimaryTaxonomyCode": "225X00000X",
      "PrimaryTaxonomy": "Occupational Therapist"
    },
    {
      "NPI": "1174191407",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "GRIMALT",
      "FirstName": "EUGENIA",
      "MiddleName": "N",
      "Credential": "PT",
      "FirstLineMailingAddress": "6396 SW MCVEY AVE",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-9069",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-389-1848",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "06/14/2021",
      "LastUpdateDate": "06/14/2021",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "2251P0200X",
      "Taxonomy1": "Pediatric Physical Therapist",
      "LicenseNumber1": "63979",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "HealthcareProviderTaxonomyGroup1": "193400000X SINGLE SPECIALTY  GROUP",
      "HealthcareProviderTaxonomyGroupDescription1": "Single Specialty Group - A business group of one or more individual practitioners, all of who practice with the same area of specialization.",
      "CertificationDate": "06/14/2021",
      "PrimaryTaxonomyCode": "2251P0200X",
      "PrimaryTaxonomy": "Pediatric Physical Therapist"
    },
    {
      "NPI": "1912604117",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "PAINTER",
      "FirstName": "JENNIFER",
      "FirstLineMailingAddress": "20080 DOANNA WAY UNIT 3",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97702-2931",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "209-743-9813",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "EnumerationDate": "02/08/2023",
      "LastUpdateDate": "02/08/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "101YM0800X",
      "Taxonomy1": "Mental Health Counselor",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "02/08/2023",
      "PrimaryTaxonomyCode": "101YM0800X",
      "PrimaryTaxonomy": "Mental Health Counselor"
    },
    {
      "NPI": "1396434700",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "GROVE",
      "FirstName": "JENNIFER",
      "MiddleName": "RHEA",
      "FirstLineMailingAddress": "303 NW BROADWAY ST",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97703-2658",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "801-573-6047",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "801-573-6047",
      "EnumerationDate": "05/02/2023",
      "LastUpdateDate": "05/02/2023",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "1041C0700X",
      "Taxonomy1": "Clinical Social Worker",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "05/02/2023",
      "PrimaryTaxonomyCode": "1041C0700X",
      "PrimaryTaxonomy": "Clinical Social Worker"
    },
    {
      "NPI": "1407698970",
      "EntityType": "Individual",
      "IsSoleProprietor": "N",
      "LastName": "REDDEN",
      "FirstName": "SHANNON",
      "Credential": "CHW",
      "OtherLastName": "MCDOUGALL",
      "OtherFirstName": "SHANNON",
      "OtherLastNameTypeCode": "1",
      "FirstLineMailingAddress": "2312 NE 5TH ST",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "OR",
      "MailingAddressPostalCode": "97756-8488",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "541-460-2192",
      "FirstLinePracticeLocationAddress": "6396 SW MCVEY AVE",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "OR",
      "PracticeLocationAddressPostalCode": "97756-9069",
      "PracticeLocationAddressCountryCode": "US",
      "PracticeLocationAddressTelephoneNumber": "541-389-1848",
      "PracticeLocationAddressFaxNumber": "541-550-7956",
      "EnumerationDate": "06/06/2024",
      "LastUpdateDate": "06/06/2024",
      "GenderCode": "F",
      "Gender": "Female",
      "TaxonomyCode1": "172V00000X",
      "Taxonomy1": "Community Health Worker",
      "LicenseNumberStateCode1": "OR",
      "PrimaryTaxonomySwitch1": "Y",
      "CertificationDate": "06/06/2024",
      "PrimaryTaxonomyCode": "172V00000X",
      "PrimaryTaxonomy": "Community Health Worker"
    },
    {
      "NPI": "1942022256",
      "EntityType": "Individual",
      "IsSoleProprietor": "Y",
      "LastName": "JACQUOT",
      "FirstName": "SHAYLA",
      "FirstLineMailingAddress": "PO BOX 1397",
      "MailingAddressCityName": "BEND",
      "MailingAddressStateName": "OR",
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}
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