43598-055-04 : NDC 2026 Code

43598-055-04 : Nilotinib ( Nilotinib )

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NDC Code : 43598-055-04 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "43598-055-04",
    "PackageDescription": "120 CAPSULE in 1 BOTTLE (43598-055-04) ",
    "NDC11Code": "43598-0055-04",
    "ProductNDC": "43598-055",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Nilotinib",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Nilotinib",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20251119",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA218350",
    "LabelerName": "Dr. Reddy&#39;s Laboratories Inc",
    "SubstanceName": "NILOTINIB HYDROCHLORIDE MONOHYDRATE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Kinase Inhibitor [EPC], P-Glycoprotein Inhibitors [MoA], UGT1A1 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-11-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251119",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}