{
"NDC": {
"NDCCode": "70000-0726-1",
"PackageDescription": "1 BOTTLE in 1 CARTON (70000-0726-1) / 180 TABLET in 1 BOTTLE",
"NDC11Code": "70000-0726-01",
"ProductNDC": "70000-0726",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "24hr Allergy Relief",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fexofenadine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20160819",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204097",
"LabelerName": "CARDINAL HEALTH 110, LLC. DBA LEADER",
"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": "2025-06-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20250509",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}