{
"NDC": {
"NDCCode": "0179-0103-80",
"PackageDescription": "2160 TABLET in 1 BOTTLE (0179-0103-80) ",
"NDC11Code": "00179-0103-80",
"ProductNDC": "0179-0103",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fenofibrate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Fenofibrate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110803",
"EndMarketingDate": "20200630",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076509",
"LabelerName": "KAISER FOUNDATION HOSPITALS",
"SubstanceName": "FENOFIBRATE",
"StrengthNumber": "54",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-07-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20110803",
"EndMarketingDatePackage": "20200630",
"SamplePackage": "N"
}
}