68071-3761-9 : NDC 2026 Code

68071-3761-9 : Febuxostat ( Febuxostat )

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NDC Code : 68071-3761-9 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68071-3761-9",
    "PackageDescription": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3761-9) ",
    "NDC11Code": "68071-3761-09",
    "ProductNDC": "68071-3761",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Febuxostat",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Febuxostat",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20210126",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA205467",
    "LabelerName": "NuCare Pharmaceuticals, Inc.",
    "SubstanceName": "FEBUXOSTAT",
    "StrengthNumber": "80",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250110",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}