60687-655-21 : NDC 2026 Code

60687-655-21 : Fenofibrate ( Fenofibrate )

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NDC Code : 60687-655-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-655-21",
    "PackageDescription": "30 BLISTER PACK in 1 CARTON (60687-655-21)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-655-11) ",
    "NDC11Code": "60687-0655-21",
    "ProductNDC": "60687-655",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221202",
    "EndMarketingDate": "20240731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076635",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "54",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-07-31",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20221202",
    "EndMarketingDatePackage": "20240731",
    "SamplePackage": "N"
  }
}