51079-321-20 : NDC 2026 Code

51079-321-20 : Finasteride ( Finasteride )

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NDC Code : 51079-321-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-321-20",
    "PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-321-20)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01) ",
    "NDC11Code": "51079-0321-20",
    "ProductNDC": "51079-321",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Finasteride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Finasteride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150713",
    "EndMarketingDate": "20190630",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077578",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "FINASTERIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-07-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20150713",
    "EndMarketingDatePackage": "20190630",
    "SamplePackage": "N"
  }
}