51655-902-52 : NDC 2026 Code

51655-902-52 : Fenofibrate ( Fenofibrate )

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NDC Code : 51655-902-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51655-902-52",
    "PackageDescription": "30 TABLET in 1 BOTTLE, DISPENSING (51655-902-52)",
    "NDC11Code": "51655-0902-52",
    "ProductNDC": "51655-902",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20150428",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA021656",
    "LabelerName": "NORTHWIND PHARMACEUTICALS",
    "SubstanceName": "FENOFIBRATE",
    "StrengthNumber": "145",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20181231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}