60687-535-65 : NDC 2026 Code

60687-535-65 : Bumetanide ( Bumetanide )

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NDC Code : 60687-535-65 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-535-65",
    "PackageDescription": "50 BLISTER PACK in 1 CARTON (60687-535-65)  / 1 TABLET in 1 BLISTER PACK (60687-535-11) ",
    "NDC11Code": "60687-0535-65",
    "ProductNDC": "60687-535",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bumetanide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bumetanide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200713",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA018225",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "BUMETANIDE",
    "StrengthNumber": "2",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-09-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240901",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}