71205-169-30 : NDC 2026 Code

71205-169-30 : Gemfibrozil ( Gemfibrozil )

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NDC Code : 71205-169-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71205-169-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (71205-169-30) ",
    "NDC11Code": "71205-0169-30",
    "ProductNDC": "71205-169",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Gemfibrozil",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Gemfibrozil",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150916",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202726",
    "LabelerName": "Proficient Rx LP",
    "SubstanceName": "GEMFIBROZIL",
    "StrengthNumber": "600",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "PPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-05-28",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20181201",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}