60760-901-30 : NDC 2026 Code

60760-901-30 : Fenofibrate ( Fenofibrate )

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NDC Code : 60760-901-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60760-901-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-901-30)",
    "NDC11Code": "60760-0901-30",
    "ProductNDC": "60760-901",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100201",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076635",
    "LabelerName": "St Marys Medical Park Pharmacy",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "160",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-01-10",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20181231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}