42292-004-08 : NDC 2026 Code

42292-004-08 : Potassium Chloride ( Potassium Chloride )

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NDC Code : 42292-004-08 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "42292-004-08",
    "PackageDescription": "80 BLISTER PACK in 1 BOX, UNIT-DOSE (42292-004-08)  &gt; 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (42292-004-01)",
    "NDC11Code": "42292-0004-08",
    "ProductNDC": "42292-004",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150430",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA204662",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "10",
    "StrengthUnit": "meq/1",
    "Pharm_Classes": "Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-04-12",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20181231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}