51079-599-20 : NDC 2026 Code

51079-599-20 : Fenofibrate ( Fenofibrate )

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NDC Code : 51079-599-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-599-20",
    "PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-599-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-599-01) ",
    "NDC11Code": "51079-0599-20",
    "ProductNDC": "51079-599",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20130610",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202856",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "48",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-07-29",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20130610",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}