{
"NDC": {
"NDCCode": "70748-172-27",
"PackageDescription": "360 TABLET in 1 BOTTLE (70748-172-27) ",
"NDC11Code": "70748-0172-27",
"ProductNDC": "70748-172",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sevelamer Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sevelamer Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20220225",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA213145",
"LabelerName": "Lupin Pharmaceuticals, Inc.",
"SubstanceName": "SEVELAMER HYDROCHLORIDE",
"StrengthNumber": "400",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-12-18",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20220225",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}