{
"NDC": {
"NDCCode": "83008-072-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (83008-072-30) ",
"NDC11Code": "83008-0072-30",
"ProductNDC": "83008-072",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fenofibrate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fenofibrate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20240711",
"EndMarketingDate": "20251031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA216798",
"LabelerName": "Quality Care Products, LLC",
"SubstanceName": "FENOFIBRATE",
"StrengthNumber": "160",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-11-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20240711",
"EndMarketingDatePackage": "20251031",
"SamplePackage": "N"
}
}