70934-298-60 : NDC 2026 Code

70934-298-60 : Fenofibrate ( Fenofibrate )

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NDC Code : 70934-298-60 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-298-60",
    "PackageDescription": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-298-60) ",
    "NDC11Code": "70934-0298-60",
    "ProductNDC": "70934-298",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20190301",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076433",
    "LabelerName": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "160",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-01-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20211231",
    "StartMarketingDatePackage": "20190301",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}