67751-033-02 : NDC 2026 Code

67751-033-02 : Fexofenadine Hydrochloride ( Allegra Allergy )

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NDC Code : 67751-033-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "67751-033-02",
    "PackageDescription": "1 BLISTER PACK in 1 CARTON (67751-033-02)  / 1 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "67751-0033-02",
    "ProductNDC": "67751-033",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Allegra Allergy",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150512",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA020872",
    "LabelerName": "Navajo Manufacturing Company 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": "2024-10-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20160331",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}