51655-554-52 : NDC 2026 Code

51655-554-52 : Fenofibrate ( Fenofibrate )

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NDC Code : 51655-554-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51655-554-52",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-554-52) ",
    "NDC11Code": "51655-0554-52",
    "ProductNDC": "51655-554",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20210121",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA200884",
    "LabelerName": "Northwind Pharmaceuticals, LLC",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "48",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20210121",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}