{
"NDC": {
"NDCCode": "68788-8819-2",
"PackageDescription": "20 TABLET in 1 BOTTLE (68788-8819-2) ",
"NDC11Code": "68788-8819-02",
"ProductNDC": "68788-8819",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Prednisone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Prednisone",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20250123",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA215672",
"LabelerName": "Preferred Pharmaceuticals Inc.",
"SubstanceName": "PREDNISONE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-01-24",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20250123",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}