35356-603-30 : NDC 2026 Code

35356-603-30 : Fenofibrate ( Fenofibrate )

Additionally :

You can get information about “35356-603-30” NDC code in 35356-603-30 in HTML format

HTML | 35356-603-30 in TXT (Plain Text) format

TXT | 35356-603-30 in PDF (Portable Document Format)

PDF | 35356-603-30 in XML format

XML formats.

NDC Code : 35356-603-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "35356-603-30",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (35356-603-30)",
    "NDC11Code": "35356-0603-30",
    "ProductNDC": "35356-603",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fenofibrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fenofibrate",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20110113",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076520",
    "LabelerName": "Lake Erie Medical &amp; Surgical Supply DBA Quality Care Products LLC",
    "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": "2018-03-16",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}