71335-0971-2 : NDC 2026 Code

71335-0971-2 : Gemfibrozil ( Gemfibrozil )

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NDC Code : 71335-0971-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71335-0971-2",
    "PackageDescription": "30 TABLET in 1 BOTTLE (71335-0971-2) ",
    "NDC11Code": "71335-0971-02",
    "ProductNDC": "71335-0971",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Gemfibrozil",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Gemfibrozil",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20101220",
    "EndMarketingDate": "20260630",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079072",
    "LabelerName": "Bryant Ranch Prepack",
    "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": "Active",
    "LastUpdate": "2024-09-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20181109",
    "EndMarketingDatePackage": "20260630",
    "SamplePackage": "N"
  }
}