{
"NDC": {
"NDCCode": "68788-7281-2",
"PackageDescription": "1 BLISTER PACK in 1 CARTON (68788-7281-2) > 21 TABLET in 1 BLISTER PACK",
"NDC11Code": "68788-7281-02",
"ProductNDC": "68788-7281",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Prednisone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Prednisone",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20190116",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA080356",
"LabelerName": "Preferred Pharmaceuticals Inc.",
"SubstanceName": "PREDNISONE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-09-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20190116",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}