21130-769-07 : NDC 2026 Code

21130-769-07 : Fexofenadine Hcl ( Fexofenadine Hcl )

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NDC Code : 21130-769-07 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "21130-769-07",
    "PackageDescription": "15 TABLET in 1 BLISTER PACK (21130-769-07) ",
    "NDC11Code": "21130-0769-07",
    "ProductNDC": "21130-769",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Fexofenadine Hcl",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hcl",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20231106",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211075",
    "LabelerName": "Safeway, Inc",
    "SubstanceName": "FEXOFENADINE HYDROCHLORIDE",
    "StrengthNumber": "180",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-23",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20231106",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}