{
"NDC": {
"NDCCode": "61748-113-48",
"PackageDescription": "48 TABLET, FILM COATED in 1 BOTTLE (61748-113-48) ",
"NDC11Code": "61748-0113-48",
"ProductNDC": "61748-113",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Demeclocycline Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Demeclocycline Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20081215",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA065389",
"LabelerName": "Versapharm Incorporated",
"SubstanceName": "DEMECLOCYCLINE HYDROCHLORIDE",
"StrengthNumber": "300",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-07-27",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20221231",
"StartMarketingDatePackage": "20081215",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}