51079-879-20 : NDC 2026 Code

51079-879-20 : Ranitidine Hydrochloride ( Ranitidine Hydrochloride )

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NDC Code : 51079-879-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-879-20",
    "PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-879-20)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-879-01)",
    "NDC11Code": "51079-0879-20",
    "ProductNDC": "51079-879",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ranitidine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ranitidine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "19970711",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA074467",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "RANITIDINE HYDROCHLORIDE",
    "StrengthNumber": "150",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-08-20",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20181231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}