60687-175-01 : NDC 2026 Code

60687-175-01 : Fexofenadine ( Fexofenadine )

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NDC Code : 60687-175-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-175-01",
    "PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-175-01)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-175-11)",
    "NDC11Code": "60687-0175-01",
    "ProductNDC": "60687-175",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Fexofenadine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160201",
    "EndMarketingDate": "20170930",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079112",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "FEXOFENADINE HYDROCHLORIDE",
    "StrengthNumber": "180",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-10-03",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}