{
"NDC": {
"NDCCode": "83114-001-01",
"PackageDescription": "1 TABLET in 1 BLISTER PACK (83114-001-01) ",
"NDC11Code": "83114-0001-01",
"ProductNDC": "83114-001",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Mifepristone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Mifepristone",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20190411",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA091178",
"LabelerName": "PCI Pharma Services Canada, Inc.",
"SubstanceName": "MIFEPRISTONE",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Progestational Hormone Receptor Antagonists [MoA], Progestin Antagonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-02-24",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20190411",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}