{
"NDC": {
"NDCCode": "55700-273-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (55700-273-30)",
"NDC11Code": "55700-0273-30",
"ProductNDC": "55700-273",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ursodiol",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ursodiol",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20111223",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA200826",
"LabelerName": "Lake Erie Medical DBA Quality Care Products LLC",
"SubstanceName": "URSODIOL",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Bile Acid [EPC],Bile Acids and Salts [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-03-21",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}