50436-0337-3 : NDC 2026 Code

50436-0337-3 : Benazepril Hydrochloride ( Benazepril Hydrochloride )

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NDC Code : 50436-0337-3 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50436-0337-3",
    "PackageDescription": "90 TABLET, COATED in 1 BOTTLE (50436-0337-3) ",
    "NDC11Code": "50436-0337-03",
    "ProductNDC": "50436-0337",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Benazepril Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Benazepril Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20140101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076118",
    "LabelerName": "Unit Dose Services",
    "SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2021-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20180927",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}