{
"NDC": {
"NDCCode": "48433-091-20",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (48433-091-20) / 1 TABLET in 1 BLISTER PACK (48433-091-01) ",
"NDC11Code": "48433-0091-20",
"ProductNDC": "48433-091",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sucralfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sucralfate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20260313",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA070848",
"LabelerName": "Safecor Health LLC",
"SubstanceName": "SUCRALFATE",
"StrengthNumber": "1",
"StrengthUnit": "g/1",
"Pharm_Classes": "Aluminum Complex [EPC], Organometallic Compounds [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-04-09",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260313",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}