{
"NDC": {
"NDCCode": "45865-845-49",
"PackageDescription": "100 TABLET in 1 BOTTLE (45865-845-49) ",
"NDC11Code": "45865-0845-49",
"ProductNDC": "45865-845",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sucralfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sucralfate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19961111",
"EndMarketingDate": "20200430",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA070848",
"LabelerName": "Medsource Pharmaceuticals",
"SubstanceName": "SUCRALFATE",
"StrengthNumber": "1",
"StrengthUnit": "g/1",
"Pharm_Classes": "Aluminum Complex [EPC],Organometallic Compounds [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-05-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20141201",
"EndMarketingDatePackage": "20200430",
"SamplePackage": "N"
}
}