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How to Find 52919-123-10 NDC Data Using DataLabs API

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{
  "NDC": [
    {
      "NDCCode": "52919-123-10",
      "PackageDescription": "1.1 mL in 1 AMPULE (52919-123-10)",
      "NDC11Code": "52919-0123-10",
      "ProductNDC": "52919-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Lymphomyosot",
      "NonProprietaryName": "Geranium Robertianum And Rorippa Nasturtium-aquaticum And Tribasic Calcium Phosphate And Levothyroxine And",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
      "StartMarketingDate": "20100401",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "GERANIUM ROBERTIANUM; RORIPPA NASTURTIUM-AQUATICUM; FERROUS IODIDE; JUGLANS REGIA FLOWERING TOP; MYOSOTIS ARVENSIS; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; VERONICA OFFICINALIS FLOWERING TOP; EQUISETUM HYEMALE; FUMARIA OFFICINALIS FLOWERING TOP; SODIUM SULFATE; PINUS SYLVESTRIS TOP; GENTIANA LUTEA ROOT; ARANEUS DIADEMATUS; SARSAPARILLA; TRIBASIC CALCIUM PHOSPHATE; LEVOTHYROXINE",
      "StrengthNumber": "4; 4; 12; 3; 3; 3; 3; 3; 4; 4; 4; 4; 5; 6; 6; 12; 12",
      "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",
      "Pharm_Classes": "Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],l-Thyroxine [EPC],Thyroxine [CS]",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "Lymphomyosot® Injection Solution is classified as a homeopathic combination drug. Botanical Ingredients:Equisetum hyemale (Horsetail), Fumaria officinalis (Common fumitory), Gentiana lutea (Yellow gentian), Geranium robertianum (Herb Robert), Juglans regia (Walnut), Myosotis arvensis (Forget-me-not), Nasturtium aquaticum (Watercress), Pinus sylvestris (Scotch Pine), Sarsaparilla (Wild liquorice), Scrophularia nodosa (Figwort), Teucrium scorodonia (Wood-germander), Veronica officinalis (Common speedwell). Mineral Ingredients:Calcarea phosphorica (Tribasic calcium phosphate), Ferrum iodatum (Ferrous iodide), Natrum sulphuricum (Disodium sulfate). Animal-derived ingredients:Aranea diadema (Papal-cross spider), Levothyroxine (L-thyroxine).",
      "Description": "Injection Solution Ingredient Information: Each 1.1ml ampule contains: Geranium robertianum 4X 1.1 mcl, Nasturtium aquaticum 4X 1.1 mcl, Ferrum iodatum 12X 1.1 mcl, Juglans regia 3X 0.55 mcl, Myosotis arvensis 3X 0.55 mcl, Scrophularia nodosa 3X 0.55 mcl, Teucrium scorodonia 3X 0.55 mcl, Veronica officinalis 3X 0.55 mcl, Equistetum hyemale 4X 0.55 mcl, Fumaria officinalis 4X 0.55 mcl, Natrum sulphuricum 4X 0.55 mcl, Pinus sylvestris 4X 0.55 mcl, Gentiana lutea 5X 0.55 mcl, Aranea diadema 6X 0.55 mcl, Sarsaparilla 6X 0.55 mcl, Calcarea phosphorica 12X 0.55 mcl, Levothyroxine 12X 0.55 mcl. Inactive Ingredients: Sterile Isotonic sodium chloride solution."
    },
    {
      "NDCCode": "0944-2948-10",
      "PackageDescription": "1 KIT in 1 CARTON (0944-2948-10)  *  5 mL in 1 VIAL, GLASS (0944-2947-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) ",
      "NDC11Code": "00944-2948-10",
      "ProductNDC": "0944-2948",
      "ProductTypeName": "PLASMA DERIVATIVE",
      "ProprietaryName": "Advate",
      "NonProprietaryName": "Antihemophilic Factor, Human Recombinant",
      "DosageFormName": "KIT",
      "StartMarketingDate": "20120712",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125063",
      "LabelerName": "Baxalta US Inc.",
      "Status": "Deprecated",
      "LastUpdate": "2018-12-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20120712",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "0944-2964-10",
      "PackageDescription": "1 KIT in 1 CARTON (0944-2964-10)  *  5 mL in 1 VIAL, GLASS (0944-2945-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) ",
      "NDC11Code": "00944-2964-10",
      "ProductNDC": "0944-2964",
      "ProductTypeName": "PLASMA DERIVATIVE",
      "ProprietaryName": "Advate",
      "NonProprietaryName": "Antihemophilic Factor, Human Recombinant",
      "DosageFormName": "KIT",
      "StartMarketingDate": "20060412",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125063",
      "LabelerName": "Baxalta US Inc.",
      "Status": "Deprecated",
      "LastUpdate": "2018-12-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20060412",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "0944-2965-10",
      "PackageDescription": "1 KIT in 1 CARTON (0944-2965-10)  *  5 mL in 1 VIAL, GLASS (0944-2946-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) ",
      "NDC11Code": "00944-2965-10",
      "ProductNDC": "0944-2965",
      "ProductTypeName": "PLASMA DERIVATIVE",
      "ProprietaryName": "Advate",
      "NonProprietaryName": "Antihemophilic Factor, Human Recombinant",
      "DosageFormName": "KIT",
      "StartMarketingDate": "20070703",
      "MarketingCategoryName": "BLA",
      "ApplicationNumber": "BLA125063",
      "LabelerName": "Baxalta US Inc.",
      "Status": "Deprecated",
      "LastUpdate": "2018-12-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20191231",
      "StartMarketingDatePackage": "20070703",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "52919-005-05",
      "PackageDescription": "50 VIAL, GLASS in 1 CARTON (52919-005-05)  / 10 mL in 1 VIAL, GLASS (52919-005-01) ",
      "NDC11Code": "52919-0005-05",
      "ProductNDC": "52919-005",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Water",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20190807",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Siegfried Hameln GmbH",
      "SubstanceName": "WATER",
      "StrengthNumber": "1",
      "StrengthUnit": "mL/mL",
      "Status": "Unfinished",
      "LastUpdate": "2025-12-16",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "07-AUG-19"
    },
    {
      "NDCCode": "52919-032-05",
      "PackageDescription": "50 VIAL, GLASS in 1 CARTON (52919-032-05)  / 10 mL in 1 VIAL, GLASS (52919-032-01) ",
      "NDC11Code": "52919-0032-05",
      "ProductNDC": "52919-032",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Water",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20230428",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Siegfried Hameln GmbH",
      "SubstanceName": "WATER",
      "StrengthNumber": "1",
      "StrengthUnit": "mL/mL",
      "Status": "Unfinished",
      "LastUpdate": "2023-05-02",
      "ListingRecordCertifiedThrough": "20241231",
      "StartMarketingDatePackage": "28-APR-23"
    },
    {
      "NDCCode": "52919-040-03",
      "PackageDescription": "10 VIAL, GLASS in 1 CARTON (52919-040-03)  / 192 mL in 1 VIAL, GLASS (52919-040-01) ",
      "NDC11Code": "52919-0040-03",
      "ProductNDC": "52919-040",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Water",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20240125",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Siegfried Hameln GmbH",
      "SubstanceName": "WATER",
      "StrengthNumber": "1",
      "StrengthUnit": "mL/mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "25-JAN-24"
    },
    {
      "NDCCode": "52919-112-10",
      "PackageDescription": "1000 AMPULE in 1 BOX (52919-112-10)  > 1.1 mL in 1 AMPULE",
      "NDC11Code": "52919-0112-10",
      "ProductNDC": "52919-112",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Cynanchum Vincetoxicum Root And Sulfur",
      "DosageFormName": "INJECTION",
      "StartMarketingDate": "20110706",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "CYNANCHUM VINCETOXICUM ROOT; SULFUR",
      "StrengthNumber": "6; 4",
      "StrengthUnit": "[hp_X]/1.1mL; [hp_X]/1.1mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-116-10",
      "PackageDescription": "1000 AMPULE in 1 BOX (52919-116-10)  > 2 mL in 1 AMPULE",
      "NDC11Code": "52919-0116-10",
      "ProductNDC": "52919-116",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": ".alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root",
      "DosageFormName": "INJECTION",
      "StartMarketingDate": "20110124",
      "EndMarketingDate": "20190531",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "THIOCTIC ACID; ARNICA MONTANA ROOT; SUS SCROFA CARTILAGE; COENZYME A; SOLANUM DULCAMARA TOP; SUS SCROFA EMBRYO; SUS SCROFA UMBILICAL CORD; NADIDE; SODIUM DIETHYL OXALACETATE; SUS SCROFA PLACENTA; TOXICODENDRON PUBESCENS LEAF; SANGUINARIA CANADENSIS ROOT; SULFUR",
      "StrengthNumber": "8; 4; 6; 8; 3; 6; 6; 8; 8; 6; 2; 4; 6",
      "StrengthUnit": "[hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04"
    },
    {
      "NDCCode": "52919-141-10",
      "PackageDescription": "1000 AMPULE in 1 BOX (52919-141-10)  > 1.1 mL in 1 AMPULE",
      "NDC11Code": "52919-0141-10",
      "ProductNDC": "52919-141",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Aconitum Napellus, Amanita Muscaria Fruiting Body,ammonium Bromide, Atropine Sulfate, Matricaria Recutita,citrullus Colocynthis Fruit Pulp,cupric Sulfate,gelsemium Sempervirens Root, Magnesium Phosphate, Dibasic Trihydrate, Passiflora Incarnata Flowering Top, And Veratrum Album Root",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20110120",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "ACONITUM NAPELLUS; AMANITA MUSCARIA FRUITING BODY; AMMONIUM BROMIDE; ATROPINE SULFATE; MATRICARIA RECUTITA; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA FLOWERING TOP; VERATRUM ALBUM ROOT",
      "StrengthNumber": "6; 4; 4; 6; 3; 4; 6; 6; 6; 2; 6",
      "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",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-161-10",
      "PackageDescription": "2.2 mL in 1 AMPULE (52919-161-10)",
      "NDC11Code": "52919-0161-10",
      "ProductNDC": "52919-161",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Traumeel",
      "NonProprietaryName": "Arnica Montana Root And Atropa Belladonna And Calendula Officinalis Flowering Top And Matricaria Recutita And Achillea Millefolium And Calcium Sulfide And Comfrey Root And Aconitum Napellus And Bellis",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
      "StartMarketingDate": "20100401",
      "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "ARNICA MONTANA ROOT; ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; COMFREY ROOT; ACONITUM NAPELLUS; BELLIS PERENNIS; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; ECHINACEA; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA LEAF",
      "StrengthNumber": "2; 2; 2; 3; 3; 6; 6; 2; 2; 6; 2; 2; 2; 1",
      "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",
      "Status": "Deprecated",
      "LastUpdate": "2017-01-20"
    },
    {
      "NDCCode": "52919-162-10",
      "PackageDescription": "1000 AMPULE in 1 BOX (52919-162-10)  > 2.2 mL in 1 AMPULE",
      "NDC11Code": "52919-0162-10",
      "ProductNDC": "52919-162",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Arnica Montana Root,atropa Belladonna, Calendula Officinalis Flowering Top,matricaria Recutita, Achillea Millefolium, Calcium Sulfide, Comfrey Root, Aconitum Napellus, Bellis Perennis, Mercurius Solubilis,hypericum Perforatum, Echinacea, Unspecified,echinacea Purpurea, And Hamamelis Virginiana Leaf",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20130117",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "ARNICA MONTANA ROOT; ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; COMFREY ROOT; ACONITUM NAPELLUS; BELLIS PERENNIS; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA LEAF",
      "StrengthNumber": "2; 2; 2; 3; 3; 6; 6; 2; 2; 6; 2; 2; 2; 1",
      "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",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-200-10",
      "PackageDescription": "1.1 mL in 1 AMPULE (52919-200-10)",
      "NDC11Code": "52919-0200-10",
      "ProductNDC": "52919-200",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root,geranium Robertianum, Myosotis Arvensis, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Regelii Root, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Thyroid, Unspecified, And Veronica Officinalis Flowering Top",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20140131",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "ARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; SODIUM SULFATE; PINUS SYLVESTRIS LEAFY TWIG; SMILAX REGELII ROOT; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; THYROID, UNSPECIFIED; VERONICA OFFICINALIS FLOWERING TOP",
      "StrengthNumber": "6; 12; 4; 12; 4; 5; 4; 3; 4; 4; 4; 6; 3; 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",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-311-10",
      "PackageDescription": "1000 AMPULE in 1 CARTON (52919-311-10)  > 2.2 mL in 1 AMPULE",
      "NDC11Code": "52919-0311-10",
      "ProductNDC": "52919-311",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Lactic Acid, L- And Viscum Album And Colchicum Autumnale Bulb And Conium Maculatum Flowering Top And Galium Aparine And Fucus Vesiculosus And Sedum Acre And Sempervivum Tectorum Leaf And Adenosine Tri",
      "DosageFormName": "INJECTION",
      "StartMarketingDate": "20110708",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "LACTIC ACID, L-; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; GALIUM APARINE; FUCUS VESICULOSUS; SEDUM ACRE; SEMPERVIVUM TECTORUM LEAF; ADENOSINE TRIPHOSPHATE; FUMARIC ACID; .ALPHA.-KETOGLUTARIC ACID; MALIC ACID; SODIUM DIETHYL OXALACETATE; PULSATILLA VULGARIS; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA THYROID; CALCIUM FLUORIDE; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; SULFUR; SUS SCROFA THYMUS; VISCUM ALBUM FRUIT; CORTISONE ACETATE",
      "StrengthNumber": "3; 4; 4; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 3; 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": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-326-10",
      "PackageDescription": "1000 AMPULE in 1 BOX (52919-326-10)  > 1.1 mL in 1 AMPULE",
      "NDC11Code": "52919-0326-10",
      "ProductNDC": "52919-326",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root",
      "DosageFormName": "INJECTION",
      "StartMarketingDate": "20110708",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Hameln Pharma GmbH",
      "SubstanceName": "PSEUDOGNAPHALIUM OBTUSIFOLIUM; CAUSTICUM; COLCHICUM AUTUMNALE BULB; CITRULLUS COLOCYNTHIS FRUIT PULP; IRON; LITHIUM BENZOATE; TOXICODENDRON PUBESCENS LEAF; FILIPENDULA ULMARIA ROOT",
      "StrengthNumber": "6; 10; 10; 10; 10; 10; 10; 10",
      "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",
      "Status": "Deprecated",
      "LastUpdate": "2014-02-04",
      "ListingRecordCertifiedThrough": "20171231"
    },
    {
      "NDCCode": "52919-021-14",
      "PackageDescription": "525 AMPULE in 1 CARTON (52919-021-14)  > 2 mL in 1 AMPULE (52919-021-01)",
      "NDC11Code": "52919-0021-14",
      "ProductNDC": "52919-021",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Polidocanol",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20100601",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Siegfried Hameln GmbH",
      "SubstanceName": "POLIDOCANOL",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Status": "Unfinished",
      "LastUpdate": "2018-10-18",
      "ListingRecordCertifiedThrough": "20191231"
    },
    {
      "NDCCode": "52919-024-14",
      "PackageDescription": "525 AMPULE in 1 CARTON (52919-024-14)  / 2 mL in 1 AMPULE (52919-024-01) ",
      "NDC11Code": "52919-0024-14",
      "ProductNDC": "52919-024",
      "ProductTypeName": "DRUG FOR FURTHER PROCESSING",
      "NonProprietaryName": "Polidocanol",
      "DosageFormName": "INJECTION, SOLUTION",
      "StartMarketingDate": "20190614",
      "MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
      "LabelerName": "Siegfried Hameln GmbH",
      "SubstanceName": "POLIDOCANOL",
      "StrengthNumber": "10",
      "StrengthUnit": "mg/mL",
      "Status": "Unfinished",
      "LastUpdate": "2024-11-20",
      "ListingRecordCertifiedThrough": "20251231",
      "StartMarketingDatePackage": "14-JUN-19"
    },
    {
      "NDCCode": "10695-123-30",
      "PackageDescription": "10 kg in 1 CONTAINER (10695-123-30) ",
      "NDC11Code": "10695-0123-30",
      "ProductNDC": "10695-123",
      "ProductTypeName": "BULK INGREDIENT",
      "NonProprietaryName": "Vardenafil Hydrochloride",
      "DosageFormName": "POWDER",
      "StartMarketingDate": "20240529",
      "MarketingCategoryName": "BULK INGREDIENT",
      "LabelerName": "Willow Birch Pharma, LLC",
      "SubstanceName": "VARDENAFIL HYDROCHLORIDE",
      "StrengthNumber": "1",
      "StrengthUnit": "kg/kg",
      "Status": "Unfinished",
      "LastUpdate": "2025-12-19",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "29-MAY-24"
    },
    {
      "NDCCode": "13107-123-10",
      "PackageDescription": "10 BLISTER PACK in 1 CARTON (13107-123-10)  > 10 TABLET, FILM COATED in 1 BLISTER PACK",
      "NDC11Code": "13107-0123-10",
      "ProductNDC": "13107-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Risperidone",
      "NonProprietaryName": "Risperidone",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20091025",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA078269",
      "LabelerName": "Aurolife Pharma LLC",
      "SubstanceName": "RISPERIDONE",
      "StrengthNumber": "3",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Atypical Antipsychotic [EPC]",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20181231"
    },
    {
      "NDCCode": "14445-123-10",
      "PackageDescription": "100 CAPSULE in 1 BLISTER PACK (14445-123-10) ",
      "NDC11Code": "14445-0123-10",
      "ProductNDC": "14445-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Pregabalin",
      "NonProprietaryName": "Pregabalin",
      "DosageFormName": "CAPSULE",
      "RouteName": "ORAL",
      "StartMarketingDate": "20240517",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA208113",
      "LabelerName": "Indoco Remedies Limited",
      "SubstanceName": "PREGABALIN",
      "StrengthNumber": "75",
      "StrengthUnit": "mg/1",
      "DEASchedule": "CV",
      "Status": "Active",
      "LastUpdate": "2025-09-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20240517",
      "SamplePackage": "N",
      "IndicationAndUsage": "Pregabalin capsules are indicated for:  Management of neuropathic pain associated with diabetic peripheral neuropathy  Management of postherpetic neuralgia  Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older Management of fibromyalgia  Management of neuropathic pain associated with spinal cord injury.",
      "Description": "Pregabalin is described chemically as (S)-3-(aminomethyl)-5-methylhexanoic acid. The molecular formula is C8H17NO2 and the molecular weight is 159.23. The chemical structure of pregabalin is:. Pregabalin is a white to off-white, crystalline solid with a pKa1 of 4.2 and a pKa2 of 10.6. It is freely soluble in water and both basic and acidic aqueous solutions. The log of the partition coefficient (n-octanol/0.05M phosphate buffer) at pH 7.4 is - 1.35. Pregabalin capsules are administered orally and are supplied as imprinted hard-shell capsules containing 25, 50, 75, 100, 150, 200, 225, and 300 mg of pregabalin, along with lactose monohydrate, cornstarch, and talc as inactive ingredients. The capsule shells contain gelatin and titanium dioxide. In addition, the orange capsule shells contain red iron oxide, sodium lauryl sulfate and colloidal silicon dioxide, water and the white capsule shells contain sodium lauryl sulfate and colloidal silicon dioxide, water. Colloidal silicon dioxide is a manufacturing aid that may or may not be present in the capsule shells. The imprinting ink contains shellac, black iron oxide, propylene glycol, and potassium hydroxide, dehydrated alcohol, isopropyl alcohol, butyl alcohol, strong ammonia solution and purified water."
    },
    {
      "NDCCode": "14789-123-05",
      "PackageDescription": "10 VIAL in 1 CARTON (14789-123-05)  / 2 mL in 1 VIAL (14789-123-07) ",
      "NDC11Code": "14789-0123-05",
      "ProductNDC": "14789-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Fluorescein",
      "NonProprietaryName": "Fluorescein",
      "DosageFormName": "INJECTION",
      "RouteName": "INTRAVENOUS",
      "StartMarketingDate": "20231024",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA215709",
      "LabelerName": "Nexus Pharmaceuticals LLC",
      "SubstanceName": "FLUORESCEIN",
      "StrengthNumber": "250",
      "StrengthUnit": "mg/mL",
      "Pharm_Classes": "Diagnostic Dye [EPC], Dyes [MoA]",
      "Status": "Active",
      "LastUpdate": "2023-10-27",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20231024",
      "SamplePackage": "N",
      "IndicationAndUsage": "Fluoresecin Injection 10%, , (100 mg/mL) and Fluorescein Injection 25% (250 mg/mL) is indicated in diagnostic fluorescein angiography or angioscopy of the retina and iris vasculature.",
      "Description": "Fluorescein Injection, is a sterile solution for use intravenously as a diagnostic aid. It is a dark reddish orange solution with a pH of 8.3 to 9.8 and an osmolality of 572 to 858 mOsm/kg for the 10% and 1800 to 2200 mOsm/kg for the 25%. Its chemical name is spiro[isobenzofuran-1 (3H),9'-[9H]xanthene]-3-one,3'6'- dihydroxy, disodium salt. The active ingredient is represented by the chemical structure:. MW = 376.27. Fluorescein Injection 10% contains:. Active: fluorescein sodium (equivalent to fluorescein 10 % w/v, 100 mg/mL). Inactives: Sodium Hydroxide and/or Hydrochloric Acid may be used to adjust pH (8.3 to 9.8), and Water for Injection. Fluorescein Injection 25% contains:. Active: fluorescein sodium (equivalent to fluorescein 25% w/v, 250 mg/mL). Inactives: Sodium Hydroxide and/or Hydrochloric Acid may be used to adjust pH (8.3 to 9.8), and Water for Injection."
    },
    {
      "NDCCode": "16729-123-10",
      "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (16729-123-10)",
      "NDC11Code": "16729-0123-10",
      "ProductNDC": "16729-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Donepezil Hydrochloride",
      "NonProprietaryName": "Donepezil Hydrochloride",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20111231",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA201335",
      "LabelerName": "Accord Healthcare, Inc.",
      "SubstanceName": "DONEPEZIL HYDROCHLORIDE",
      "StrengthNumber": "5",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2015-05-15"
    },
    {
      "NDCCode": "16729-123-44",
      "PackageDescription": "10 BLISTER PACK in 1 CARTON (16729-123-44)  > 10 TABLET, FILM COATED in 1 BLISTER PACK",
      "NDC11Code": "16729-0123-44",
      "ProductNDC": "16729-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Donepezil Hydrochloride",
      "NonProprietaryName": "Donepezil Hydrochloride",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20111231",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA201335",
      "LabelerName": "Accord Healthcare, Inc.",
      "SubstanceName": "DONEPEZIL HYDROCHLORIDE",
      "StrengthNumber": "5",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]",
      "Status": "Deprecated",
      "LastUpdate": "2015-05-15"
    },
    {
      "NDCCode": "17772-123-10",
      "PackageDescription": "5 TABLET in 1 BLISTER PACK (17772-123-10) ",
      "NDC11Code": "17772-0123-10",
      "ProductNDC": "17772-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Oxtellar Xr",
      "NonProprietaryName": "Oxcarbazepine",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20130117",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA202810",
      "LabelerName": "Supernus Pharmaceuticals, Inc.",
      "SubstanceName": "OXCARBAZEPINE",
      "StrengthNumber": "600",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]",
      "Status": "Active",
      "LastUpdate": "2025-10-23",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20130117",
      "SamplePackage": "Y",
      "IndicationAndUsage": "Oxtellar XR is indicated for the treatment of partial-onset seizures in patients 6 years of age and older.",
      "Description": "Oxtellar XR is an antiepileptic drug (AED). Oxtellar XR extended-release tablets contain oxcarbazepine for once-a-day oral administration. Oxcarbazepine is 10,11-Dihydro-10-oxo-5H-dibenz[b,f]-azepine-5-carboxamide, and its structural formula is. Oxcarbazepine is off-white to yellow crystalline powder. Oxcarbazepine is sparingly soluble in chloroform (30-100 g/L). In aqueous media over pH range 1 to 8, oxcarbazepine is practically insoluble and its solubility is 40 mg/L (0.04 g/L) at pH 7.0, 25°C. The molecular formula is C 15H 12N 2O 2and its molecular weight is 252.27. Oxtellar XR tablets contain the following inactive ingredients: colloidal silicon dioxide, hypromellose, yellow iron oxide (150 mg, 300 mg tablets only), red iron oxide (300 mg, 600 mg tablets only), black iron oxide (300 mg tablet only), magnesium stearate, methacrylic acid copolymer, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, sodium lauryl sulfate, talc, and titanium dioxide. Each tablet is printed on one side with edible black ink."
    },
    {
      "NDCCode": "21220-123-10",
      "PackageDescription": "196 L in 1 DEWAR (21220-123-10) ",
      "NDC11Code": "21220-0123-10",
      "ProductNDC": "21220-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Carbon Dioxide",
      "NonProprietaryName": "Carbon Dioxide",
      "DosageFormName": "GAS",
      "RouteName": "RESPIRATORY (INHALATION)",
      "StartMarketingDate": "19720601",
      "MarketingCategoryName": "NDA",
      "ApplicationNumber": "NDA207166",
      "LabelerName": "General Air Service & Supply Co.",
      "SubstanceName": "CARBON DIOXIDE",
      "StrengthNumber": "990",
      "StrengthUnit": "mL/L",
      "Pharm_Classes": "Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]",
      "Status": "Active",
      "LastUpdate": "2025-11-28",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "19720601",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "24765-123-10",
      "PackageDescription": "15 mL in 1 BOTTLE (24765-123-10) ",
      "NDC11Code": "24765-0123-10",
      "ProductNDC": "24765-123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Mycellcare It S",
      "NonProprietaryName": "Propylen Glycol Glycerin Allantoin",
      "DosageFormName": "SPRAY",
      "RouteName": "TOPICAL",
      "StartMarketingDate": "20180618",
      "MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
      "ApplicationNumber": "part334",
      "LabelerName": "Pharmacal International Co.,Ltd.",
      "SubstanceName": "PROPYLENE GLYCOL; GLYCERIN; ALLANTOIN",
      "StrengthNumber": "50; 20; 5",
      "StrengthUnit": "mg/mL; mg/mL; mg/mL",
      "Status": "Deprecated",
      "LastUpdate": "2021-06-05",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20211231",
      "StartMarketingDatePackage": "20180618",
      "SamplePackage": "N"
    },
    {
      "NDCCode": "33342-123-12",
      "PackageDescription": "10 BLISTER PACK in 1 CARTON (33342-123-12)  / 10 TABLET in 1 BLISTER PACK",
      "NDC11Code": "33342-0123-12",
      "ProductNDC": "33342-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Aripiprazole",
      "NonProprietaryName": "Aripiprazole",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20161008",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA204111",
      "LabelerName": "Macleods Pharmaceuticals Limited",
      "SubstanceName": "ARIPIPRAZOLE",
      "StrengthNumber": "5",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Atypical Antipsychotic [EPC]",
      "Status": "Active",
      "LastUpdate": "2025-04-02",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20161008",
      "SamplePackage": "N",
      "IndicationAndUsage": "Aripiprazole Tablets are indicated for the treatment of: Schizophrenia.  Irritability Associated with Autistic Disorder Treatment of Tourette’s Disorder.",
      "Description": "Aripiprazole, USP is an atypical antipsychotic drug that is available as aripiprazole tablets, USP. Aripiprazole, USP is 7-[4-[4-(2,3-dichlorophenyl)-1piperazinyl]butoxy]-3,4-dihydrocarbostyril. The empirical formula is C23H27C12N3O2 and its molecular weight is 448.38. The chemical structure is. Aripiprazole tablets, USP are available in 2 mg, 5 mg, 10 mg, 15 mg, 20 mg, and 30 mg strengths. Inactive ingredients include corn starch, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. Colorants include ferric oxide (yellow or red) and FD&C Blue No. 2 Aluminum Lake."
    },
    {
      "NDCCode": "41250-123-20",
      "PackageDescription": "10 POUCH in 1 CARTON (41250-123-20)  / 2 TABLET, EFFERVESCENT in 1 POUCH",
      "NDC11Code": "41250-0123-20",
      "ProductNDC": "41250-123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Effervescent Orange Cold Relief",
      "NonProprietaryName": "Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate",
      "DosageFormName": "TABLET, EFFERVESCENT",
      "RouteName": "ORAL",
      "StartMarketingDate": "20130526",
      "MarketingCategoryName": "OTC MONOGRAPH DRUG",
      "ApplicationNumber": "M012",
      "LabelerName": "Meijer Distribution Inc.",
      "SubstanceName": "PHENYLEPHRINE BITARTRATE; ASPIRIN; CHLORPHENIRAMINE MALEATE",
      "StrengthNumber": "7.8; 325; 2",
      "StrengthUnit": "mg/1; mg/1; mg/1",
      "Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], alpha-1 Adrenergic Agonist [EPC]",
      "Status": "Active",
      "LastUpdate": "2025-02-04",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20130526",
      "EndMarketingDatePackage": "20261231",
      "SamplePackage": "N",
      "IndicationAndUsage": "â–  temporarily relieves these symptoms due to the common cold. â–  sneezing â–  nasal congestion â–  sore throat â–  headache. â–  minor aches and pains â–  runny nose â–  sinus congestion and pressure. â–  temporarily reduces fever."
    },
    {
      "NDCCode": "42254-123-10",
      "PackageDescription": "10 TABLET, FILM COATED in 1 BOTTLE (42254-123-10)",
      "NDC11Code": "42254-0123-10",
      "ProductNDC": "42254-123",
      "ProductTypeName": "HUMAN OTC DRUG",
      "ProprietaryName": "Fexofenadine Hydrochloride",
      "NonProprietaryName": "Fexofenadine Hcl",
      "DosageFormName": "TABLET, FILM COATED",
      "RouteName": "ORAL",
      "StartMarketingDate": "20110808",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA076447",
      "LabelerName": "Rebel Distributors Corp",
      "SubstanceName": "FEXOFENADINE HYDROCHLORIDE",
      "StrengthNumber": "60",
      "StrengthUnit": "mg/1",
      "Status": "Deprecated",
      "LastUpdate": "2019-09-21",
      "ProductNdcExcludeFlag": "E",
      "ListingRecordCertifiedThrough": "20171231",
      "IndicationAndUsage": "temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: 1 runny nose , 2 itchy, watery eyes , 3 sneezing , 4 itching of the nose or throat."
    },
    {
      "NDCCode": "42806-123-10",
      "PackageDescription": "1000 TABLET in 1 BOTTLE (42806-123-10) ",
      "NDC11Code": "42806-0123-10",
      "ProductNDC": "42806-123",
      "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
      "ProprietaryName": "Sotalol Hydrochloride",
      "NonProprietaryName": "Sotalol Hydrochloride",
      "DosageFormName": "TABLET",
      "RouteName": "ORAL",
      "StartMarketingDate": "20160104",
      "MarketingCategoryName": "ANDA",
      "ApplicationNumber": "ANDA077070",
      "LabelerName": "Epic Pharma, LLC",
      "SubstanceName": "SOTALOL HYDROCHLORIDE",
      "StrengthNumber": "160",
      "StrengthUnit": "mg/1",
      "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]",
      "Status": "Active",
      "LastUpdate": "2025-12-19",
      "PackageNdcExcludeFlag": "N",
      "ProductNdcExcludeFlag": "N",
      "ListingRecordCertifiedThrough": "20261231",
      "StartMarketingDatePackage": "20160104",
      "SamplePackage": "N",
      "IndicationAndUsage": "Sotalol hydrochloride tablets (AF) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).",
      "Description": "Sotalol hydrochloride tablets, USP (AF) contains sotalol hydrochloride, an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. It is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol, and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S·HCl and is represented by the following structural formula. Sotalol hydrochloride tablets, USP (AF) contain the following inactive ingredients: pregelatinized starch, microcrystalline cellulose, lactose monohydrate, colloidal silicon dioxide, stearic acid, and magnesium stearate."
    }
  ]
}
                    
{"NDC":[{"NDCCode":"52919-123-10","ProprietaryName":"Lymphomyosot","NonProprietaryName":"Geranium Robertianum And Rorippa Nasturtium-aquaticum And Tribasic Calcium Phosphate And Levothyroxine And"},{"NDCCode":"0944-2948-10","ProprietaryName":"Advate","NonProprietaryName":"Antihemophilic Factor, Human Recombinant"},{"NDCCode":"0944-2964-10","ProprietaryName":"Advate","NonProprietaryName":"Antihemophilic Factor, Human Recombinant"},{"NDCCode":"0944-2965-10","ProprietaryName":"Advate","NonProprietaryName":"Antihemophilic Factor, Human Recombinant"},{"NDCCode":"52919-005-05","NonProprietaryName":"Water"},{"NDCCode":"52919-032-05","NonProprietaryName":"Water"},{"NDCCode":"52919-040-03","NonProprietaryName":"Water"},{"NDCCode":"52919-112-10","NonProprietaryName":"Cynanchum Vincetoxicum Root And Sulfur"},{"NDCCode":"52919-116-10","NonProprietaryName":".alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root"},{"NDCCode":"52919-141-10","NonProprietaryName":"Aconitum Napellus, Amanita Muscaria Fruiting Body,ammonium Bromide, Atropine Sulfate, Matricaria Recutita,citrullus Colocynthis Fruit Pulp,cupric Sulfate,gelsemium Sempervirens Root, Magnesium Phosphate, Dibasic Trihydrate, Passiflora Incarnata Flowering Top, And Veratrum Album Root"},{"NDCCode":"52919-161-10","ProprietaryName":"Traumeel","NonProprietaryName":"Arnica Montana Root And Atropa Belladonna And Calendula Officinalis Flowering Top And Matricaria Recutita And Achillea Millefolium And Calcium Sulfide And Comfrey Root And Aconitum Napellus And Bellis"},{"NDCCode":"52919-162-10","NonProprietaryName":"Arnica Montana Root,atropa Belladonna, Calendula Officinalis Flowering Top,matricaria Recutita, Achillea Millefolium, Calcium Sulfide, Comfrey Root, Aconitum Napellus, Bellis Perennis, Mercurius Solubilis,hypericum Perforatum, Echinacea, Unspecified,echinacea Purpurea, And Hamamelis Virginiana Leaf"},{"NDCCode":"52919-200-10","NonProprietaryName":"Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root,geranium Robertianum, Myosotis Arvensis, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Regelii Root, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Thyroid, Unspecified, And Veronica Officinalis Flowering Top"},{"NDCCode":"52919-311-10","NonProprietaryName":"Lactic Acid, L- And Viscum Album And Colchicum Autumnale Bulb And Conium Maculatum Flowering Top And Galium Aparine And Fucus Vesiculosus And Sedum Acre And Sempervivum Tectorum Leaf And Adenosine Tri"},{"NDCCode":"52919-326-10","NonProprietaryName":"Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root"},{"NDCCode":"52919-021-14","NonProprietaryName":"Polidocanol"},{"NDCCode":"52919-024-14","NonProprietaryName":"Polidocanol"},{"NDCCode":"10695-123-30","NonProprietaryName":"Vardenafil Hydrochloride"},{"NDCCode":"13107-123-10","ProprietaryName":"Risperidone","NonProprietaryName":"Risperidone"},{"NDCCode":"14445-123-10","ProprietaryName":"Pregabalin","NonProprietaryName":"Pregabalin"},{"NDCCode":"14789-123-05","ProprietaryName":"Fluorescein","NonProprietaryName":"Fluorescein"},{"NDCCode":"16729-123-10","ProprietaryName":"Donepezil Hydrochloride","NonProprietaryName":"Donepezil Hydrochloride"},{"NDCCode":"16729-123-44","ProprietaryName":"Donepezil Hydrochloride","NonProprietaryName":"Donepezil Hydrochloride"},{"NDCCode":"17772-123-10","ProprietaryName":"Oxtellar Xr","NonProprietaryName":"Oxcarbazepine"},{"NDCCode":"21220-123-10","ProprietaryName":"Carbon Dioxide","NonProprietaryName":"Carbon Dioxide"},{"NDCCode":"24765-123-10","ProprietaryName":"Mycellcare It S","NonProprietaryName":"Propylen Glycol Glycerin Allantoin"},{"NDCCode":"33342-123-12","ProprietaryName":"Aripiprazole","NonProprietaryName":"Aripiprazole"},{"NDCCode":"41250-123-20","ProprietaryName":"Effervescent Orange Cold Relief","NonProprietaryName":"Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate"},{"NDCCode":"42254-123-10","ProprietaryName":"Fexofenadine Hydrochloride","NonProprietaryName":"Fexofenadine Hcl"},{"NDCCode":"42806-123-10","ProprietaryName":"Sotalol Hydrochloride","NonProprietaryName":"Sotalol Hydrochloride"}]}
                    
<?xml version="1.0" encoding="utf-8"?>
<NDCList>
  <NDC>
    <NDCCode>52919-123-10</NDCCode>
    <PackageDescription>1.1 mL in 1 AMPULE (52919-123-10)</PackageDescription>
    <NDC11Code>52919-0123-10</NDC11Code>
    <ProductNDC>52919-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Lymphomyosot</ProprietaryName>
    <NonProprietaryName>Geranium Robertianum And Rorippa Nasturtium-aquaticum And Tribasic Calcium Phosphate And Levothyroxine And</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20100401</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>GERANIUM ROBERTIANUM; RORIPPA NASTURTIUM-AQUATICUM; FERROUS IODIDE; JUGLANS REGIA FLOWERING TOP; MYOSOTIS ARVENSIS; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; VERONICA OFFICINALIS FLOWERING TOP; EQUISETUM HYEMALE; FUMARIA OFFICINALIS FLOWERING TOP; SODIUM SULFATE; PINUS SYLVESTRIS TOP; GENTIANA LUTEA ROOT; ARANEUS DIADEMATUS; SARSAPARILLA; TRIBASIC CALCIUM PHOSPHATE; LEVOTHYROXINE</SubstanceName>
    <StrengthNumber>4; 4; 12; 3; 3; 3; 3; 3; 4; 4; 4; 4; 5; 6; 6; 12; 12</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</StrengthUnit>
    <Pharm_Classes>Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS],l-Thyroxine [EPC],Thyroxine [CS]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>Lymphomyosot® Injection Solution is classified as a homeopathic combination drug. Botanical Ingredients:Equisetum hyemale (Horsetail), Fumaria officinalis (Common fumitory), Gentiana lutea (Yellow gentian), Geranium robertianum (Herb Robert), Juglans regia (Walnut), Myosotis arvensis (Forget-me-not), Nasturtium aquaticum (Watercress), Pinus sylvestris (Scotch Pine), Sarsaparilla (Wild liquorice), Scrophularia nodosa (Figwort), Teucrium scorodonia (Wood-germander), Veronica officinalis (Common speedwell). Mineral Ingredients:Calcarea phosphorica (Tribasic calcium phosphate), Ferrum iodatum (Ferrous iodide), Natrum sulphuricum (Disodium sulfate). Animal-derived ingredients:Aranea diadema (Papal-cross spider), Levothyroxine (L-thyroxine).</IndicationAndUsage>
    <Description>Injection Solution Ingredient Information: Each 1.1ml ampule contains: Geranium robertianum 4X 1.1 mcl, Nasturtium aquaticum 4X 1.1 mcl, Ferrum iodatum 12X 1.1 mcl, Juglans regia 3X 0.55 mcl, Myosotis arvensis 3X 0.55 mcl, Scrophularia nodosa 3X 0.55 mcl, Teucrium scorodonia 3X 0.55 mcl, Veronica officinalis 3X 0.55 mcl, Equistetum hyemale 4X 0.55 mcl, Fumaria officinalis 4X 0.55 mcl, Natrum sulphuricum 4X 0.55 mcl, Pinus sylvestris 4X 0.55 mcl, Gentiana lutea 5X 0.55 mcl, Aranea diadema 6X 0.55 mcl, Sarsaparilla 6X 0.55 mcl, Calcarea phosphorica 12X 0.55 mcl, Levothyroxine 12X 0.55 mcl. Inactive Ingredients: Sterile Isotonic sodium chloride solution.</Description>
  </NDC>
  <NDC>
    <NDCCode>0944-2948-10</NDCCode>
    <PackageDescription>1 KIT in 1 CARTON (0944-2948-10)  *  5 mL in 1 VIAL, GLASS (0944-2947-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) </PackageDescription>
    <NDC11Code>00944-2948-10</NDC11Code>
    <ProductNDC>0944-2948</ProductNDC>
    <ProductTypeName>PLASMA DERIVATIVE</ProductTypeName>
    <ProprietaryName>Advate</ProprietaryName>
    <NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName>
    <DosageFormName>KIT</DosageFormName>
    <StartMarketingDate>20120712</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125063</ApplicationNumber>
    <LabelerName>Baxalta US Inc.</LabelerName>
    <Status>Deprecated</Status>
    <LastUpdate>2018-12-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20120712</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>0944-2964-10</NDCCode>
    <PackageDescription>1 KIT in 1 CARTON (0944-2964-10)  *  5 mL in 1 VIAL, GLASS (0944-2945-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) </PackageDescription>
    <NDC11Code>00944-2964-10</NDC11Code>
    <ProductNDC>0944-2964</ProductNDC>
    <ProductTypeName>PLASMA DERIVATIVE</ProductTypeName>
    <ProprietaryName>Advate</ProprietaryName>
    <NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName>
    <DosageFormName>KIT</DosageFormName>
    <StartMarketingDate>20060412</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125063</ApplicationNumber>
    <LabelerName>Baxalta US Inc.</LabelerName>
    <Status>Deprecated</Status>
    <LastUpdate>2018-12-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20060412</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>0944-2965-10</NDCCode>
    <PackageDescription>1 KIT in 1 CARTON (0944-2965-10)  *  5 mL in 1 VIAL, GLASS (0944-2946-01)  *  5 mL in 1 VIAL, GLASS (52919-003-08) </PackageDescription>
    <NDC11Code>00944-2965-10</NDC11Code>
    <ProductNDC>0944-2965</ProductNDC>
    <ProductTypeName>PLASMA DERIVATIVE</ProductTypeName>
    <ProprietaryName>Advate</ProprietaryName>
    <NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName>
    <DosageFormName>KIT</DosageFormName>
    <StartMarketingDate>20070703</StartMarketingDate>
    <MarketingCategoryName>BLA</MarketingCategoryName>
    <ApplicationNumber>BLA125063</ApplicationNumber>
    <LabelerName>Baxalta US Inc.</LabelerName>
    <Status>Deprecated</Status>
    <LastUpdate>2018-12-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20070703</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>52919-005-05</NDCCode>
    <PackageDescription>50 VIAL, GLASS in 1 CARTON (52919-005-05)  / 10 mL in 1 VIAL, GLASS (52919-005-01) </PackageDescription>
    <NDC11Code>52919-0005-05</NDC11Code>
    <ProductNDC>52919-005</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Water</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20190807</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Siegfried Hameln GmbH</LabelerName>
    <SubstanceName>WATER</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mL/mL</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2025-12-16</LastUpdate>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>07-AUG-19</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>52919-032-05</NDCCode>
    <PackageDescription>50 VIAL, GLASS in 1 CARTON (52919-032-05)  / 10 mL in 1 VIAL, GLASS (52919-032-01) </PackageDescription>
    <NDC11Code>52919-0032-05</NDC11Code>
    <ProductNDC>52919-032</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Water</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20230428</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Siegfried Hameln GmbH</LabelerName>
    <SubstanceName>WATER</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mL/mL</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2023-05-02</LastUpdate>
    <ListingRecordCertifiedThrough>20241231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>28-APR-23</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>52919-040-03</NDCCode>
    <PackageDescription>10 VIAL, GLASS in 1 CARTON (52919-040-03)  / 192 mL in 1 VIAL, GLASS (52919-040-01) </PackageDescription>
    <NDC11Code>52919-0040-03</NDC11Code>
    <ProductNDC>52919-040</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Water</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20240125</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Siegfried Hameln GmbH</LabelerName>
    <SubstanceName>WATER</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>mL/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>25-JAN-24</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>52919-112-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 BOX (52919-112-10)  &gt; 1.1 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0112-10</NDC11Code>
    <ProductNDC>52919-112</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Cynanchum Vincetoxicum Root And Sulfur</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <StartMarketingDate>20110706</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>CYNANCHUM VINCETOXICUM ROOT; SULFUR</SubstanceName>
    <StrengthNumber>6; 4</StrengthNumber>
    <StrengthUnit>[hp_X]/1.1mL; [hp_X]/1.1mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-116-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 BOX (52919-116-10)  &gt; 2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0116-10</NDC11Code>
    <ProductNDC>52919-116</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>.alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <StartMarketingDate>20110124</StartMarketingDate>
    <EndMarketingDate>20190531</EndMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>THIOCTIC ACID; ARNICA MONTANA ROOT; SUS SCROFA CARTILAGE; COENZYME A; SOLANUM DULCAMARA TOP; SUS SCROFA EMBRYO; SUS SCROFA UMBILICAL CORD; NADIDE; SODIUM DIETHYL OXALACETATE; SUS SCROFA PLACENTA; TOXICODENDRON PUBESCENS LEAF; SANGUINARIA CANADENSIS ROOT; SULFUR</SubstanceName>
    <StrengthNumber>8; 4; 6; 8; 3; 6; 6; 8; 8; 6; 2; 4; 6</StrengthNumber>
    <StrengthUnit>[hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>52919-141-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 BOX (52919-141-10)  &gt; 1.1 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0141-10</NDC11Code>
    <ProductNDC>52919-141</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Aconitum Napellus, Amanita Muscaria Fruiting Body,ammonium Bromide, Atropine Sulfate, Matricaria Recutita,citrullus Colocynthis Fruit Pulp,cupric Sulfate,gelsemium Sempervirens Root, Magnesium Phosphate, Dibasic Trihydrate, Passiflora Incarnata Flowering Top, And Veratrum Album Root</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20110120</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>ACONITUM NAPELLUS; AMANITA MUSCARIA FRUITING BODY; AMMONIUM BROMIDE; ATROPINE SULFATE; MATRICARIA RECUTITA; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC SULFATE; GELSEMIUM SEMPERVIRENS ROOT; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PASSIFLORA INCARNATA FLOWERING TOP; VERATRUM ALBUM ROOT</SubstanceName>
    <StrengthNumber>6; 4; 4; 6; 3; 4; 6; 6; 6; 2; 6</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</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-161-10</NDCCode>
    <PackageDescription>2.2 mL in 1 AMPULE (52919-161-10)</PackageDescription>
    <NDC11Code>52919-0161-10</NDC11Code>
    <ProductNDC>52919-161</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Traumeel</ProprietaryName>
    <NonProprietaryName>Arnica Montana Root And Atropa Belladonna And Calendula Officinalis Flowering Top And Matricaria Recutita And Achillea Millefolium And Calcium Sulfide And Comfrey Root And Aconitum Napellus And Bellis</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS</RouteName>
    <StartMarketingDate>20100401</StartMarketingDate>
    <MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>ARNICA MONTANA ROOT; ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; COMFREY ROOT; ACONITUM NAPELLUS; BELLIS PERENNIS; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; ECHINACEA; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA LEAF</SubstanceName>
    <StrengthNumber>2; 2; 2; 3; 3; 6; 6; 2; 2; 6; 2; 2; 2; 1</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</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2017-01-20</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>52919-162-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 BOX (52919-162-10)  &gt; 2.2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0162-10</NDC11Code>
    <ProductNDC>52919-162</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Arnica Montana Root,atropa Belladonna, Calendula Officinalis Flowering Top,matricaria Recutita, Achillea Millefolium, Calcium Sulfide, Comfrey Root, Aconitum Napellus, Bellis Perennis, Mercurius Solubilis,hypericum Perforatum, Echinacea, Unspecified,echinacea Purpurea, And Hamamelis Virginiana Leaf</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20130117</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>ARNICA MONTANA ROOT; ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; COMFREY ROOT; ACONITUM NAPELLUS; BELLIS PERENNIS; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA LEAF</SubstanceName>
    <StrengthNumber>2; 2; 2; 3; 3; 6; 6; 2; 2; 6; 2; 2; 2; 1</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</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-200-10</NDCCode>
    <PackageDescription>1.1 mL in 1 AMPULE (52919-200-10)</PackageDescription>
    <NDC11Code>52919-0200-10</NDC11Code>
    <ProductNDC>52919-200</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root,geranium Robertianum, Myosotis Arvensis, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Regelii Root, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Thyroid, Unspecified, And Veronica Officinalis Flowering Top</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20140131</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>ARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; SODIUM SULFATE; PINUS SYLVESTRIS LEAFY TWIG; SMILAX REGELII ROOT; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; THYROID, UNSPECIFIED; VERONICA OFFICINALIS FLOWERING TOP</SubstanceName>
    <StrengthNumber>6; 12; 4; 12; 4; 5; 4; 3; 4; 4; 4; 6; 3; 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</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-311-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 CARTON (52919-311-10)  &gt; 2.2 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0311-10</NDC11Code>
    <ProductNDC>52919-311</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Lactic Acid, L- And Viscum Album And Colchicum Autumnale Bulb And Conium Maculatum Flowering Top And Galium Aparine And Fucus Vesiculosus And Sedum Acre And Sempervivum Tectorum Leaf And Adenosine Tri</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <StartMarketingDate>20110708</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>LACTIC ACID, L-; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; GALIUM APARINE; FUCUS VESICULOSUS; SEDUM ACRE; SEMPERVIVUM TECTORUM LEAF; ADENOSINE TRIPHOSPHATE; FUMARIC ACID; .ALPHA.-KETOGLUTARIC ACID; MALIC ACID; SODIUM DIETHYL OXALACETATE; PULSATILLA VULGARIS; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA THYROID; CALCIUM FLUORIDE; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; SULFUR; SUS SCROFA THYMUS; VISCUM ALBUM FRUIT; CORTISONE ACETATE</SubstanceName>
    <StrengthNumber>3; 4; 4; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 3; 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>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-326-10</NDCCode>
    <PackageDescription>1000 AMPULE in 1 BOX (52919-326-10)  &gt; 1.1 mL in 1 AMPULE</PackageDescription>
    <NDC11Code>52919-0326-10</NDC11Code>
    <ProductNDC>52919-326</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <StartMarketingDate>20110708</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Hameln Pharma GmbH</LabelerName>
    <SubstanceName>PSEUDOGNAPHALIUM OBTUSIFOLIUM; CAUSTICUM; COLCHICUM AUTUMNALE BULB; CITRULLUS COLOCYNTHIS FRUIT PULP; IRON; LITHIUM BENZOATE; TOXICODENDRON PUBESCENS LEAF; FILIPENDULA ULMARIA ROOT</SubstanceName>
    <StrengthNumber>6; 10; 10; 10; 10; 10; 10; 10</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</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2014-02-04</LastUpdate>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-021-14</NDCCode>
    <PackageDescription>525 AMPULE in 1 CARTON (52919-021-14)  &gt; 2 mL in 1 AMPULE (52919-021-01)</PackageDescription>
    <NDC11Code>52919-0021-14</NDC11Code>
    <ProductNDC>52919-021</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Polidocanol</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20100601</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Siegfried Hameln GmbH</LabelerName>
    <SubstanceName>POLIDOCANOL</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2018-10-18</LastUpdate>
    <ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>52919-024-14</NDCCode>
    <PackageDescription>525 AMPULE in 1 CARTON (52919-024-14)  / 2 mL in 1 AMPULE (52919-024-01) </PackageDescription>
    <NDC11Code>52919-0024-14</NDC11Code>
    <ProductNDC>52919-024</ProductNDC>
    <ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
    <NonProprietaryName>Polidocanol</NonProprietaryName>
    <DosageFormName>INJECTION, SOLUTION</DosageFormName>
    <StartMarketingDate>20190614</StartMarketingDate>
    <MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
    <LabelerName>Siegfried Hameln GmbH</LabelerName>
    <SubstanceName>POLIDOCANOL</SubstanceName>
    <StrengthNumber>10</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2024-11-20</LastUpdate>
    <ListingRecordCertifiedThrough>20251231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>14-JUN-19</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>10695-123-30</NDCCode>
    <PackageDescription>10 kg in 1 CONTAINER (10695-123-30) </PackageDescription>
    <NDC11Code>10695-0123-30</NDC11Code>
    <ProductNDC>10695-123</ProductNDC>
    <ProductTypeName>BULK INGREDIENT</ProductTypeName>
    <NonProprietaryName>Vardenafil Hydrochloride</NonProprietaryName>
    <DosageFormName>POWDER</DosageFormName>
    <StartMarketingDate>20240529</StartMarketingDate>
    <MarketingCategoryName>BULK INGREDIENT</MarketingCategoryName>
    <LabelerName>Willow Birch Pharma, LLC</LabelerName>
    <SubstanceName>VARDENAFIL HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>1</StrengthNumber>
    <StrengthUnit>kg/kg</StrengthUnit>
    <Status>Unfinished</Status>
    <LastUpdate>2025-12-19</LastUpdate>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>29-MAY-24</StartMarketingDatePackage>
  </NDC>
  <NDC>
    <NDCCode>13107-123-10</NDCCode>
    <PackageDescription>10 BLISTER PACK in 1 CARTON (13107-123-10)  &gt; 10 TABLET, FILM COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>13107-0123-10</NDC11Code>
    <ProductNDC>13107-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Risperidone</ProprietaryName>
    <NonProprietaryName>Risperidone</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20091025</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA078269</ApplicationNumber>
    <LabelerName>Aurolife Pharma LLC</LabelerName>
    <SubstanceName>RISPERIDONE</SubstanceName>
    <StrengthNumber>3</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Atypical Antipsychotic [EPC]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
  </NDC>
  <NDC>
    <NDCCode>14445-123-10</NDCCode>
    <PackageDescription>100 CAPSULE in 1 BLISTER PACK (14445-123-10) </PackageDescription>
    <NDC11Code>14445-0123-10</NDC11Code>
    <ProductNDC>14445-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Pregabalin</ProprietaryName>
    <NonProprietaryName>Pregabalin</NonProprietaryName>
    <DosageFormName>CAPSULE</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20240517</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA208113</ApplicationNumber>
    <LabelerName>Indoco Remedies Limited</LabelerName>
    <SubstanceName>PREGABALIN</SubstanceName>
    <StrengthNumber>75</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <DEASchedule>CV</DEASchedule>
    <Status>Active</Status>
    <LastUpdate>2025-09-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20240517</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Pregabalin capsules are indicated for:  Management of neuropathic pain associated with diabetic peripheral neuropathy  Management of postherpetic neuralgia  Adjunctive therapy for the treatment of partial-onset seizures in patients 1 month of age and older Management of fibromyalgia  Management of neuropathic pain associated with spinal cord injury.</IndicationAndUsage>
    <Description>Pregabalin is described chemically as (S)-3-(aminomethyl)-5-methylhexanoic acid. The molecular formula is C8H17NO2 and the molecular weight is 159.23. The chemical structure of pregabalin is:. Pregabalin is a white to off-white, crystalline solid with a pKa1 of 4.2 and a pKa2 of 10.6. It is freely soluble in water and both basic and acidic aqueous solutions. The log of the partition coefficient (n-octanol/0.05M phosphate buffer) at pH 7.4 is - 1.35. Pregabalin capsules are administered orally and are supplied as imprinted hard-shell capsules containing 25, 50, 75, 100, 150, 200, 225, and 300 mg of pregabalin, along with lactose monohydrate, cornstarch, and talc as inactive ingredients. The capsule shells contain gelatin and titanium dioxide. In addition, the orange capsule shells contain red iron oxide, sodium lauryl sulfate and colloidal silicon dioxide, water and the white capsule shells contain sodium lauryl sulfate and colloidal silicon dioxide, water. Colloidal silicon dioxide is a manufacturing aid that may or may not be present in the capsule shells. The imprinting ink contains shellac, black iron oxide, propylene glycol, and potassium hydroxide, dehydrated alcohol, isopropyl alcohol, butyl alcohol, strong ammonia solution and purified water.</Description>
  </NDC>
  <NDC>
    <NDCCode>14789-123-05</NDCCode>
    <PackageDescription>10 VIAL in 1 CARTON (14789-123-05)  / 2 mL in 1 VIAL (14789-123-07) </PackageDescription>
    <NDC11Code>14789-0123-05</NDC11Code>
    <ProductNDC>14789-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Fluorescein</ProprietaryName>
    <NonProprietaryName>Fluorescein</NonProprietaryName>
    <DosageFormName>INJECTION</DosageFormName>
    <RouteName>INTRAVENOUS</RouteName>
    <StartMarketingDate>20231024</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA215709</ApplicationNumber>
    <LabelerName>Nexus Pharmaceuticals LLC</LabelerName>
    <SubstanceName>FLUORESCEIN</SubstanceName>
    <StrengthNumber>250</StrengthNumber>
    <StrengthUnit>mg/mL</StrengthUnit>
    <Pharm_Classes>Diagnostic Dye [EPC], Dyes [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2023-10-27</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20231024</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Fluoresecin Injection 10%, , (100 mg/mL) and Fluorescein Injection 25% (250 mg/mL) is indicated in diagnostic fluorescein angiography or angioscopy of the retina and iris vasculature.</IndicationAndUsage>
    <Description>Fluorescein Injection, is a sterile solution for use intravenously as a diagnostic aid. It is a dark reddish orange solution with a pH of 8.3 to 9.8 and an osmolality of 572 to 858 mOsm/kg for the 10% and 1800 to 2200 mOsm/kg for the 25%. Its chemical name is spiro[isobenzofuran-1 (3H),9'-[9H]xanthene]-3-one,3'6'- dihydroxy, disodium salt. The active ingredient is represented by the chemical structure:. MW = 376.27. Fluorescein Injection 10% contains:. Active: fluorescein sodium (equivalent to fluorescein 10 % w/v, 100 mg/mL). Inactives: Sodium Hydroxide and/or Hydrochloric Acid may be used to adjust pH (8.3 to 9.8), and Water for Injection. Fluorescein Injection 25% contains:. Active: fluorescein sodium (equivalent to fluorescein 25% w/v, 250 mg/mL). Inactives: Sodium Hydroxide and/or Hydrochloric Acid may be used to adjust pH (8.3 to 9.8), and Water for Injection.</Description>
  </NDC>
  <NDC>
    <NDCCode>16729-123-10</NDCCode>
    <PackageDescription>30 TABLET, FILM COATED in 1 BOTTLE (16729-123-10)</PackageDescription>
    <NDC11Code>16729-0123-10</NDC11Code>
    <ProductNDC>16729-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Donepezil Hydrochloride</ProprietaryName>
    <NonProprietaryName>Donepezil Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20111231</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA201335</ApplicationNumber>
    <LabelerName>Accord Healthcare, Inc.</LabelerName>
    <SubstanceName>DONEPEZIL HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>5</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2015-05-15</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>16729-123-44</NDCCode>
    <PackageDescription>10 BLISTER PACK in 1 CARTON (16729-123-44)  &gt; 10 TABLET, FILM COATED in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>16729-0123-44</NDC11Code>
    <ProductNDC>16729-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Donepezil Hydrochloride</ProprietaryName>
    <NonProprietaryName>Donepezil Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20111231</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA201335</ApplicationNumber>
    <LabelerName>Accord Healthcare, Inc.</LabelerName>
    <SubstanceName>DONEPEZIL HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>5</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]</Pharm_Classes>
    <Status>Deprecated</Status>
    <LastUpdate>2015-05-15</LastUpdate>
  </NDC>
  <NDC>
    <NDCCode>17772-123-10</NDCCode>
    <PackageDescription>5 TABLET in 1 BLISTER PACK (17772-123-10) </PackageDescription>
    <NDC11Code>17772-0123-10</NDC11Code>
    <ProductNDC>17772-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Oxtellar Xr</ProprietaryName>
    <NonProprietaryName>Oxcarbazepine</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20130117</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA202810</ApplicationNumber>
    <LabelerName>Supernus Pharmaceuticals, Inc.</LabelerName>
    <SubstanceName>OXCARBAZEPINE</SubstanceName>
    <StrengthNumber>600</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-10-23</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20130117</StartMarketingDatePackage>
    <SamplePackage>Y</SamplePackage>
    <IndicationAndUsage>Oxtellar XR is indicated for the treatment of partial-onset seizures in patients 6 years of age and older.</IndicationAndUsage>
    <Description>Oxtellar XR is an antiepileptic drug (AED). Oxtellar XR extended-release tablets contain oxcarbazepine for once-a-day oral administration. Oxcarbazepine is 10,11-Dihydro-10-oxo-5H-dibenz[b,f]-azepine-5-carboxamide, and its structural formula is. Oxcarbazepine is off-white to yellow crystalline powder. Oxcarbazepine is sparingly soluble in chloroform (30-100 g/L). In aqueous media over pH range 1 to 8, oxcarbazepine is practically insoluble and its solubility is 40 mg/L (0.04 g/L) at pH 7.0, 25°C. The molecular formula is C 15H 12N 2O 2and its molecular weight is 252.27. Oxtellar XR tablets contain the following inactive ingredients: colloidal silicon dioxide, hypromellose, yellow iron oxide (150 mg, 300 mg tablets only), red iron oxide (300 mg, 600 mg tablets only), black iron oxide (300 mg tablet only), magnesium stearate, methacrylic acid copolymer, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, sodium lauryl sulfate, talc, and titanium dioxide. Each tablet is printed on one side with edible black ink.</Description>
  </NDC>
  <NDC>
    <NDCCode>21220-123-10</NDCCode>
    <PackageDescription>196 L in 1 DEWAR (21220-123-10) </PackageDescription>
    <NDC11Code>21220-0123-10</NDC11Code>
    <ProductNDC>21220-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Carbon Dioxide</ProprietaryName>
    <NonProprietaryName>Carbon Dioxide</NonProprietaryName>
    <DosageFormName>GAS</DosageFormName>
    <RouteName>RESPIRATORY (INHALATION)</RouteName>
    <StartMarketingDate>19720601</StartMarketingDate>
    <MarketingCategoryName>NDA</MarketingCategoryName>
    <ApplicationNumber>NDA207166</ApplicationNumber>
    <LabelerName>General Air Service &amp; Supply Co.</LabelerName>
    <SubstanceName>CARBON DIOXIDE</SubstanceName>
    <StrengthNumber>990</StrengthNumber>
    <StrengthUnit>mL/L</StrengthUnit>
    <Pharm_Classes>Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-11-28</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>19720601</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>24765-123-10</NDCCode>
    <PackageDescription>15 mL in 1 BOTTLE (24765-123-10) </PackageDescription>
    <NDC11Code>24765-0123-10</NDC11Code>
    <ProductNDC>24765-123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Mycellcare It S</ProprietaryName>
    <NonProprietaryName>Propylen Glycol Glycerin Allantoin</NonProprietaryName>
    <DosageFormName>SPRAY</DosageFormName>
    <RouteName>TOPICAL</RouteName>
    <StartMarketingDate>20180618</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
    <ApplicationNumber>part334</ApplicationNumber>
    <LabelerName>Pharmacal International Co.,Ltd.</LabelerName>
    <SubstanceName>PROPYLENE GLYCOL; GLYCERIN; ALLANTOIN</SubstanceName>
    <StrengthNumber>50; 20; 5</StrengthNumber>
    <StrengthUnit>mg/mL; mg/mL; mg/mL</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2021-06-05</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20211231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20180618</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
  </NDC>
  <NDC>
    <NDCCode>33342-123-12</NDCCode>
    <PackageDescription>10 BLISTER PACK in 1 CARTON (33342-123-12)  / 10 TABLET in 1 BLISTER PACK</PackageDescription>
    <NDC11Code>33342-0123-12</NDC11Code>
    <ProductNDC>33342-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Aripiprazole</ProprietaryName>
    <NonProprietaryName>Aripiprazole</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20161008</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA204111</ApplicationNumber>
    <LabelerName>Macleods Pharmaceuticals Limited</LabelerName>
    <SubstanceName>ARIPIPRAZOLE</SubstanceName>
    <StrengthNumber>5</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Atypical Antipsychotic [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-04-02</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20161008</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Aripiprazole Tablets are indicated for the treatment of: Schizophrenia.  Irritability Associated with Autistic Disorder Treatment of Tourette’s Disorder.</IndicationAndUsage>
    <Description>Aripiprazole, USP is an atypical antipsychotic drug that is available as aripiprazole tablets, USP. Aripiprazole, USP is 7-[4-[4-(2,3-dichlorophenyl)-1piperazinyl]butoxy]-3,4-dihydrocarbostyril. The empirical formula is C23H27C12N3O2 and its molecular weight is 448.38. The chemical structure is. Aripiprazole tablets, USP are available in 2 mg, 5 mg, 10 mg, 15 mg, 20 mg, and 30 mg strengths. Inactive ingredients include corn starch, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, and microcrystalline cellulose. Colorants include ferric oxide (yellow or red) and FD&amp;C Blue No. 2 Aluminum Lake.</Description>
  </NDC>
  <NDC>
    <NDCCode>41250-123-20</NDCCode>
    <PackageDescription>10 POUCH in 1 CARTON (41250-123-20)  / 2 TABLET, EFFERVESCENT in 1 POUCH</PackageDescription>
    <NDC11Code>41250-0123-20</NDC11Code>
    <ProductNDC>41250-123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Effervescent Orange Cold Relief</ProprietaryName>
    <NonProprietaryName>Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate</NonProprietaryName>
    <DosageFormName>TABLET, EFFERVESCENT</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20130526</StartMarketingDate>
    <MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
    <ApplicationNumber>M012</ApplicationNumber>
    <LabelerName>Meijer Distribution Inc.</LabelerName>
    <SubstanceName>PHENYLEPHRINE BITARTRATE; ASPIRIN; CHLORPHENIRAMINE MALEATE</SubstanceName>
    <StrengthNumber>7.8; 325; 2</StrengthNumber>
    <StrengthUnit>mg/1; mg/1; mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC], alpha-1 Adrenergic Agonist [EPC]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-02-04</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20130526</StartMarketingDatePackage>
    <EndMarketingDatePackage>20261231</EndMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>â–  temporarily relieves these symptoms due to the common cold. â–  sneezing â–  nasal congestion â–  sore throat â–  headache. â–  minor aches and pains â–  runny nose â–  sinus congestion and pressure. â–  temporarily reduces fever.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>42254-123-10</NDCCode>
    <PackageDescription>10 TABLET, FILM COATED in 1 BOTTLE (42254-123-10)</PackageDescription>
    <NDC11Code>42254-0123-10</NDC11Code>
    <ProductNDC>42254-123</ProductNDC>
    <ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
    <ProprietaryName>Fexofenadine Hydrochloride</ProprietaryName>
    <NonProprietaryName>Fexofenadine Hcl</NonProprietaryName>
    <DosageFormName>TABLET, FILM COATED</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20110808</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA076447</ApplicationNumber>
    <LabelerName>Rebel Distributors Corp</LabelerName>
    <SubstanceName>FEXOFENADINE HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>60</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Status>Deprecated</Status>
    <LastUpdate>2019-09-21</LastUpdate>
    <ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
    <IndicationAndUsage>temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: 1 runny nose , 2 itchy, watery eyes , 3 sneezing , 4 itching of the nose or throat.</IndicationAndUsage>
  </NDC>
  <NDC>
    <NDCCode>42806-123-10</NDCCode>
    <PackageDescription>1000 TABLET in 1 BOTTLE (42806-123-10) </PackageDescription>
    <NDC11Code>42806-0123-10</NDC11Code>
    <ProductNDC>42806-123</ProductNDC>
    <ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
    <ProprietaryName>Sotalol Hydrochloride</ProprietaryName>
    <NonProprietaryName>Sotalol Hydrochloride</NonProprietaryName>
    <DosageFormName>TABLET</DosageFormName>
    <RouteName>ORAL</RouteName>
    <StartMarketingDate>20160104</StartMarketingDate>
    <MarketingCategoryName>ANDA</MarketingCategoryName>
    <ApplicationNumber>ANDA077070</ApplicationNumber>
    <LabelerName>Epic Pharma, LLC</LabelerName>
    <SubstanceName>SOTALOL HYDROCHLORIDE</SubstanceName>
    <StrengthNumber>160</StrengthNumber>
    <StrengthUnit>mg/1</StrengthUnit>
    <Pharm_Classes>Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]</Pharm_Classes>
    <Status>Active</Status>
    <LastUpdate>2025-12-19</LastUpdate>
    <PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
    <ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
    <ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
    <StartMarketingDatePackage>20160104</StartMarketingDatePackage>
    <SamplePackage>N</SamplePackage>
    <IndicationAndUsage>Sotalol hydrochloride tablets (AF) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).</IndicationAndUsage>
    <Description>Sotalol hydrochloride tablets, USP (AF) contains sotalol hydrochloride, an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. It is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol, and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S·HCl and is represented by the following structural formula. Sotalol hydrochloride tablets, USP (AF) contain the following inactive ingredients: pregelatinized starch, microcrystalline cellulose, lactose monohydrate, colloidal silicon dioxide, stearic acid, and magnesium stearate.</Description>
  </NDC>
</NDCList>
                    
<NDCList><NDC><NDCCode>52919-123-10</NDCCode><ProprietaryName>Lymphomyosot</ProprietaryName><NonProprietaryName>Geranium Robertianum And Rorippa Nasturtium-aquaticum And Tribasic Calcium Phosphate And Levothyroxine And</NonProprietaryName></NDC><NDC><NDCCode>0944-2948-10</NDCCode><ProprietaryName>Advate</ProprietaryName><NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName></NDC><NDC><NDCCode>0944-2964-10</NDCCode><ProprietaryName>Advate</ProprietaryName><NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName></NDC><NDC><NDCCode>0944-2965-10</NDCCode><ProprietaryName>Advate</ProprietaryName><NonProprietaryName>Antihemophilic Factor, Human Recombinant</NonProprietaryName></NDC><NDC><NDCCode>52919-005-05</NDCCode><NonProprietaryName>Water</NonProprietaryName></NDC><NDC><NDCCode>52919-032-05</NDCCode><NonProprietaryName>Water</NonProprietaryName></NDC><NDC><NDCCode>52919-040-03</NDCCode><NonProprietaryName>Water</NonProprietaryName></NDC><NDC><NDCCode>52919-112-10</NDCCode><NonProprietaryName>Cynanchum Vincetoxicum Root And Sulfur</NonProprietaryName></NDC><NDC><NDCCode>52919-116-10</NDCCode><NonProprietaryName>.alpha.-lipoic Acid, Arnica Montana Root, Sus Scrofa Cartilage, Coenzyme A, Solanum Dulcamara Top, Sus Scrofa Embryo, Sus Scrofa Umbilical Cord, Nadide, Sodium Diethyl Oxalacetate, Sus Scrofa Placenta, Toxicodendron Pubescens Leaf, Sanguinaria Canadensis Root, Sulfur And Comfrey Root</NonProprietaryName></NDC><NDC><NDCCode>52919-141-10</NDCCode><NonProprietaryName>Aconitum Napellus, Amanita Muscaria Fruiting Body,ammonium Bromide, Atropine Sulfate, Matricaria Recutita,citrullus Colocynthis Fruit Pulp,cupric Sulfate,gelsemium Sempervirens Root, Magnesium Phosphate, Dibasic Trihydrate, Passiflora Incarnata Flowering Top, And Veratrum Album Root</NonProprietaryName></NDC><NDC><NDCCode>52919-161-10</NDCCode><ProprietaryName>Traumeel</ProprietaryName><NonProprietaryName>Arnica Montana Root And Atropa Belladonna And Calendula Officinalis Flowering Top And Matricaria Recutita And Achillea Millefolium And Calcium Sulfide And Comfrey Root And Aconitum Napellus And Bellis</NonProprietaryName></NDC><NDC><NDCCode>52919-162-10</NDCCode><NonProprietaryName>Arnica Montana Root,atropa Belladonna, Calendula Officinalis Flowering Top,matricaria Recutita, Achillea Millefolium, Calcium Sulfide, Comfrey Root, Aconitum Napellus, Bellis Perennis, Mercurius Solubilis,hypericum Perforatum, Echinacea, Unspecified,echinacea Purpurea, And Hamamelis Virginiana Leaf</NonProprietaryName></NDC><NDC><NDCCode>52919-200-10</NDCCode><NonProprietaryName>Araneus Diadematus, Tribasic Calcium Phosphate, Equisetum Hyemale, Ferrous Iodide, Fumaria Officinalis Flowering Top, Gentiana Lutea Root,geranium Robertianum, Myosotis Arvensis, Nasturtium Officinale, Sodium Sulfate, Pinus Sylvestris Leafy Twig, Smilax Regelii Root, Scrophularia Nodosa, Teucrium Scorodonia Flowering Top, Thyroid, Unspecified, And Veronica Officinalis Flowering Top</NonProprietaryName></NDC><NDC><NDCCode>52919-311-10</NDCCode><NonProprietaryName>Lactic Acid, L- And Viscum Album And Colchicum Autumnale Bulb And Conium Maculatum Flowering Top And Galium Aparine And Fucus Vesiculosus And Sedum Acre And Sempervivum Tectorum Leaf And Adenosine Tri</NonProprietaryName></NDC><NDC><NDCCode>52919-326-10</NDCCode><NonProprietaryName>Pseudognaphalium Obtusifolium And Causticum And Colchicum Autumnale Bulb And Citrullus Colocynthis Fruit Pulp And Iron And Lithium Benzoate And Toxicodendron Pubescens Leaf And Filipendula Ulmaria Root</NonProprietaryName></NDC><NDC><NDCCode>52919-021-14</NDCCode><NonProprietaryName>Polidocanol</NonProprietaryName></NDC><NDC><NDCCode>52919-024-14</NDCCode><NonProprietaryName>Polidocanol</NonProprietaryName></NDC><NDC><NDCCode>10695-123-30</NDCCode><NonProprietaryName>Vardenafil Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>13107-123-10</NDCCode><ProprietaryName>Risperidone</ProprietaryName><NonProprietaryName>Risperidone</NonProprietaryName></NDC><NDC><NDCCode>14445-123-10</NDCCode><ProprietaryName>Pregabalin</ProprietaryName><NonProprietaryName>Pregabalin</NonProprietaryName></NDC><NDC><NDCCode>14789-123-05</NDCCode><ProprietaryName>Fluorescein</ProprietaryName><NonProprietaryName>Fluorescein</NonProprietaryName></NDC><NDC><NDCCode>16729-123-10</NDCCode><ProprietaryName>Donepezil Hydrochloride</ProprietaryName><NonProprietaryName>Donepezil Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>16729-123-44</NDCCode><ProprietaryName>Donepezil Hydrochloride</ProprietaryName><NonProprietaryName>Donepezil Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>17772-123-10</NDCCode><ProprietaryName>Oxtellar Xr</ProprietaryName><NonProprietaryName>Oxcarbazepine</NonProprietaryName></NDC><NDC><NDCCode>21220-123-10</NDCCode><ProprietaryName>Carbon Dioxide</ProprietaryName><NonProprietaryName>Carbon Dioxide</NonProprietaryName></NDC><NDC><NDCCode>24765-123-10</NDCCode><ProprietaryName>Mycellcare It S</ProprietaryName><NonProprietaryName>Propylen Glycol Glycerin Allantoin</NonProprietaryName></NDC><NDC><NDCCode>33342-123-12</NDCCode><ProprietaryName>Aripiprazole</ProprietaryName><NonProprietaryName>Aripiprazole</NonProprietaryName></NDC><NDC><NDCCode>41250-123-20</NDCCode><ProprietaryName>Effervescent Orange Cold Relief</ProprietaryName><NonProprietaryName>Aspirin, Chlorpheniramine Maleate, Phenylephrine Bitartrate</NonProprietaryName></NDC><NDC><NDCCode>42254-123-10</NDCCode><ProprietaryName>Fexofenadine Hydrochloride</ProprietaryName><NonProprietaryName>Fexofenadine Hcl</NonProprietaryName></NDC><NDC><NDCCode>42806-123-10</NDCCode><ProprietaryName>Sotalol Hydrochloride</ProprietaryName><NonProprietaryName>Sotalol Hydrochloride</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.

Parameter Meaning Notes
domain Domain
  • Currently following data domains are supported:
    • NPI - NPI Number Lookup
    • HCPCS - Healthcare Provider Procedure Coding System Lookup
    • NDC - National Drug Code Lookup
    • NDCA - Animal Drug Product Listing Directory Lookup
    • CLIA - Clinical Laboratory Improvement Amendments
    • HPTC - Healthcare Provider Taxonomy Code Lookup
    • NAICS - North American Industry Classification System Lookup
    • LOINC - Logical Observation Identifiers Names and Codes (LOINC®) Lookup
    • DRG - Diagnosis-Related Group Lookup
    • ICD9 - Ninth Revision of the International Classification of Diseases Lookup
    • ICD10 - Tenth Revision of the International Classification of Diseases Lookup
    • ICD10DRUGS - ICD-10-CM Table Of Drugs And Chemicals Lookup
    • ZIP - Postal Codes used by the United States Postal Service
operation Operation
  • Generic operations:
    • check_status - this method allows to get current code status.
    • search - allows retrieval of set of items (up to 30) 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.
    • 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.
  • 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.
q Query
  • The search expression. May vary depending on the operation.
    • Free form text like: “q=blood glucose monitor” (search operation)
    • Exact code value : “q=1285636522” (getcode operation)
    • List of codes : “q=1285636522,1730198755,1427145176,1487730636” (getcodes operation)
zipcode Query for NPI by Zip code/radius Lookup
  • The search expression for zip code.
    • Exact code value : “zipcode=98052” (search operation)
radius Query for NPI by Zip code/radius Lookup
  • The search expression for radius.
    • Exact code value : “radius=20” (search operation)
fromdate Query for Deactivated NPI
  • The search expression for fromdate.
    • Exact code value : “fromdate=05/01/2023” (search operation - format MM/DD/YYYY)
todate Query for Deactivated NPI
  • The search expression for tomdate.
    • Exact code value : “todate=05/31/2023” (search operation - format MM/DD/YYYY)
tin Query for IRS Lookup
  • The search expression for tin number.
    • Exact code value : “tin=942404110” (search operation)
tinname Query for IRS Lookup
  • The search expression for tin name.
    • Free form text like: “tinname=apple inc.” (search operation)
rt Data format
  • If you don't specify an rt parameter, the API returns data in the JSON format. This is equivalent to rt=json.
  • Accepted values are:
    • json
    • minjson (minified json)
    • xml
    • minxml (minified xml)
token Your API key
num Number of search results to return
  • You can specify the how many results to return for the current search.
  • Valid values are integers between 1 and 100, inclusive.
  • If num is not used, a value of 30 is assumed.
friendlyprint Returns a response with indentations and line breaks
  • If friendlyprint is not used, a “true” value is assumed. This is equivalent to friendlyprint=true.
  • Accepted values are:
    • true - the results returned by the server will be more “human readable”.
    • false - the results returned by the server will not have indentations and line breaks.
ICD9/ICD10 Parameters
codeType Specifies whether ICD code is "dx"(Diagnosis) or "pcs"(Procedure).
  • Required for ICD only.
  • If you don't specify an codeType parameter this is equivalent to codeType=dx.
  • Accepted values are:
    • dx (diagnosis)
    • pcs (procedure)
qf Specifies predicate in form of tuple "qf=City:true:Phoenix".
  • Expected to be one or many "qf" parameters in request.
  • Required for following operations:
    • validate
    • paginate_with_predicates
    • search_with_predicates
  • Tuple values are (order based):
    • NPI Field Name
      • NPI
      • Phone
      • Fax
      • FirstName
      • LastName
      • OrganizationName
      • OtherOrganizationName
      • Address1
      • Address2
      • Zip
      • City
      • State
      • IndividualOrganizationCode
    • Exact Match
      • true
      • false
    • Expected Field Value
orderField Sort order field name
  • Expected to be one "orderField" parameter in request.
  • Required for following operations:
    • paginate_with_predicates
  • Values are:
    • NPI
    • Phone
    • Fax
    • FirstName
    • LastName
    • OrganizationName
    • OtherOrganizationName
    • Address1
    • Address2
    • Zip
    • City
    • State
    • IndividualOrganizationCode
pageNo Page Number
  • Ordinal page number.
  • Required for following operations:
    • paginate_with_predicates
    • zipradius
    • npideactivated
pageSize Page Size
  • Expected page size.
  • Required for following operations:
    • paginate_with_predicates

DataLabs Coding Library - Quering NPI Registry - REST API Examples

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();
    }
}
            
        

Output

            
{
  "NPI": [
    {
      "NPI": "1295783033",
      "EntityType": "Organization",
      "EIN": "N/A",
      "IsOrgSubpart": "N",
      "OrgName": "REDMOND EYE DOCTORS, PLLC",
      "FirstLineMailingAddress": "16375 NE 85TH ST",
      "SecondLineMailingAddress": "SUITE 102",
      "MailingAddressCityName": "REDMOND",
      "MailingAddressStateName": "WA",
      "MailingAddressPostalCode": "98052-3554",
      "MailingAddressCountryCode": "US",
      "MailingAddressTelephoneNumber": "425-885-7363",
      "MailingAddressFaxNumber": "425-861-5585",
      "FirstLinePracticeLocationAddress": "16375 NE 85TH ST",
      "SecondLinePracticeLocationAddress": "SUITE 102",
      "PracticeLocationAddressCityName": "REDMOND",
      "PracticeLocationAddressStateName": "WA",
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      "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 ...
            
        

Full Text Search Fundamentals

Facts

Everybody uses full text search. Full-text search is the most common technique used in search engines. The amount of information has just become too much to access it using navigation and categories alone. Full-text search reduces the hassle of searching for a keyword in huge amounts of metadata, such as the World Wide Web and commercial-scale databases. Full-text search became popular in late 1990s, when the Internet and Big Data began to became a part of everyday life.

How does it work

Users only provide keywords and expect the search engine to provide good results. Relevancy of documents is expected to be good and users want the results they are looking to be present in the top ten. How relevant a document is search engine decides based on scientifically proven algorithms. Besides getting the best results the user wants to be supported during the search process. Features like suggestions and highlighting on the result excerpt can help with this.

Full Text Search & DataLabs REST API

DataLabs REST API allows you to search the full text of healthcare providers database (NPI Registry). To find the information you need and make your search easy, please use our REST API for automation, or visit our NPI Lookup page for manual search ( NPI Number Lookup). We are still improving and enhancing Full Text NPI Search based on users feedbacks. Please email your comments and suggestions for improvement using our feedback page.

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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
    {
      "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();
        }
    }
                
            

Output

                
{
  "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",
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}
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