{
"NDC": {
"NDCCode": "71626-902-05",
"PackageDescription": "5 mL in 1 CUP, UNIT-DOSE (71626-902-05) ",
"NDC11Code": "71626-0902-05",
"ProductNDC": "71626-902",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Prednisolone Sodium Phosphate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Prednisolone Sodium Phosphate",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20170131",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078988",
"LabelerName": "Medstone Pharma LLC",
"SubstanceName": "PREDNISOLONE SODIUM PHOSPHATE",
"StrengthNumber": "20",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-05-15",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20170131",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}