72579-122-01 : NDC 2025 Code

72579-122-01 : Zanubrutinib ( Brukinsa )

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NDC Code : 72579-122-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72579-122-01",
    "PackageDescription": "1 BOTTLE in 1 CARTON (72579-122-01)  / 60 TABLET, FILM COATED in 1 BOTTLE",
    "NDC11Code": "72579-0122-01",
    "ProductNDC": "72579-122",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Brukinsa",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Zanubrutinib",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250818",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA218785",
    "LabelerName": "BeOne Medicines USA, Inc.",
    "SubstanceName": "ZANUBRUTINIB",
    "StrengthNumber": "160",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bruton&#39;s Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-06",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250818",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}