{
"NDC": {
"NDCCode": "0378-7291-89",
"PackageDescription": "50 TABLET in 1 BOTTLE (0378-7291-89) ",
"NDC11Code": "00378-7291-89",
"ProductNDC": "0378-7291",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Norethindrone Acetate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Norethindrone Acetate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20190719",
"EndMarketingDate": "20251130",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA205278",
"LabelerName": "Mylan Pharmaceuticals Inc.",
"SubstanceName": "NORETHINDRONE ACETATE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Progesterone Congeners [CS], Progestin [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-12-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20190719",
"EndMarketingDatePackage": "20251130",
"SamplePackage": "N"
}
}