72319-003-60 : NDC 2026 Code

72319-003-60 : Everolimus ( Everolimus )

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NDC Code : 72319-003-60 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72319-003-60",
    "PackageDescription": "60 BLISTER PACK in 1 CARTON (72319-003-60)  / 10 TABLET in 1 BLISTER PACK (72319-003-10) ",
    "NDC11Code": "72319-0003-60",
    "ProductNDC": "72319-003",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Everolimus",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Everolimus",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260807",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA219464",
    "LabelerName": "i3 Pharmaceuticals, LLC",
    "SubstanceName": "EVEROLIMUS",
    "StrengthNumber": ".25",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-09-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260807",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}