30142-878-64 : NDC 2026 Code

30142-878-64 : Fexofenadine Hydrochloride ( Fexofenadine Hydrochloride )

Additionally :

You can get information about “30142-878-64” NDC code in 30142-878-64 in HTML format

HTML | 30142-878-64 in TXT (Plain Text) format

TXT | 30142-878-64 in PDF (Portable Document Format)

PDF | 30142-878-64 in XML format

XML formats.

NDC Code : 30142-878-64 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "30142-878-64",
    "PackageDescription": "2 BOTTLE in 1 CARTON (30142-878-64)  / 70 TABLET in 1 BOTTLE",
    "NDC11Code": "30142-0878-64",
    "ProductNDC": "30142-878",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Fexofenadine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fexofenadine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20180930",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076502",
    "LabelerName": "KROGER COMPANY",
    "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": "2024-11-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20190110",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}