{
"NDC": {
"NDCCode": "52536-008-03",
"PackageDescription": "30 TABLET in 1 BOTTLE (52536-008-03) ",
"NDC11Code": "52536-0008-03",
"ProductNDC": "52536-008",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Azilsartan Medoxomil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Azilsartan Kamedoxomil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20260427",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA200796",
"LabelerName": "Wilshire 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": "2026-04-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260427",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}