{
"NDC": {
"NDCCode": "70748-237-06",
"PackageDescription": "30 TABLET in 1 BOTTLE (70748-237-06) ",
"NDC11Code": "70748-0237-06",
"ProductNDC": "70748-237",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Azilsartan Medoxomil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Azilsartan Medoxomil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20260514",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA214489",
"LabelerName": "Lupin Pharmaceuticals, Inc.",
"SubstanceName": "AZILSARTAN KAMEDOXOMIL",
"StrengthNumber": "80",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Angiotensin 2 Receptor Blocker [EPC], Angiotensin 2 Type 1 Receptor Antagonists [MoA], Decreased Blood Pressure [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-05-15",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260514",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}