{
"NDC": {
"NDCCode": "60687-130-25",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-130-25) / 1 TABLET in 1 BLISTER PACK (60687-130-95) ",
"NDC11Code": "60687-0130-25",
"ProductNDC": "60687-130",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Candesartan Cilexetil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Candesartan Cilexetil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20151102",
"EndMarketingDate": "20250831",
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA020838",
"LabelerName": "American Health Packaging",
"SubstanceName": "CANDESARTAN CILEXETIL",
"StrengthNumber": "32",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-09-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20151102",
"EndMarketingDatePackage": "20250831",
"SamplePackage": "N"
}
}