60687-241-25 : NDC 2026 Code

60687-241-25 : Candesartan Cilexetil ( Candesartan Cilexetil )

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NDC Code : 60687-241-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-241-25",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-241-25)  / 1 TABLET in 1 BLISTER PACK (60687-241-95) ",
    "NDC11Code": "60687-0241-25",
    "ProductNDC": "60687-241",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Candesartan Cilexetil",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Candesartan Cilexetil",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20161007",
    "EndMarketingDate": "20250930",
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA020838",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "CANDESARTAN CILEXETIL",
    "StrengthNumber": "16",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-10-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20161007",
    "EndMarketingDatePackage": "20250930",
    "SamplePackage": "N"
  }
}