70518-2971-0 : NDC 2026 Code

70518-2971-0 : Fexofenadine Hydrochloride ( Fexofenadine Hydrochloride )

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NDC Code : 70518-2971-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-2971-0",
    "PackageDescription": "100 TABLET in 1 BOTTLE, PLASTIC (70518-2971-0) ",
    "NDC11Code": "70518-2971-00",
    "ProductNDC": "70518-2971",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Fexofenadine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20201216",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076502",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "FEXOFENADINE HYDROCHLORIDE",
    "StrengthNumber": "180",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-01-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20231231",
    "StartMarketingDatePackage": "20201216",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}