{
"NDC": {
"NDCCode": "70518-1250-0",
"PackageDescription": "30 TABLET in 1 BLISTER PACK (70518-1250-0) ",
"NDC11Code": "70518-1250-00",
"ProductNDC": "70518-1250",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Digoxin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Digoxin",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180611",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077002",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "DIGOXIN",
"StrengthNumber": "125",
"StrengthUnit": "ug/1",
"Pharm_Classes": "Cardiac Glycoside [EPC],Cardiac Glycosides [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20180611",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}