{
"NDC": {
"NDCCode": "42291-296-90",
"PackageDescription": "90 TABLET, FILM COATED in 1 BOTTLE (42291-296-90) ",
"NDC11Code": "42291-0296-90",
"ProductNDC": "42291-296",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Fexofenadine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fexofenadine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20151016",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA202039",
"LabelerName": "AvKARE, Inc.",
"SubstanceName": "FEXOFENADINE HYDROCHLORIDE",
"StrengthNumber": "60",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-08-22",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20151016",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}