49999-772-30 : NDC 2026 Code

49999-772-30 : Fexofenadine Hydrochloride ( Fexofenadine Hydrochloride )

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NDC Code : 49999-772-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "49999-772-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49999-772-30)",
    "NDC11Code": "49999-0772-30",
    "ProductNDC": "49999-772",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fexofenadine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20050801",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA020872",
    "LabelerName": "Lake Erie Medical DBA Quality Care Products LLC",
    "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": "2017-02-03",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}