NDC 72579-122-01
BRUKINSA 160 mg/1
zanubrutinib · TABLET, FILM COATED
BRUKINSA is a tablet, film coated containing zanubrutinib at a strength of 160 mg/1. Manufactured by BeOne Medicines USA, Inc..
Key Facts
- Brand Name
- BRUKINSA
- Generic Name
- zanubrutinib
- NDC Code (Package)
72579-122-01- NDC Code (Product)
72579-122- Manufacturer
- BeOne Medicines USA, Inc.
- Strength
- 160 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA218785
- Drug Class
- Kinase Inhibitor [EPC]
- Marketing Start
- 08/18/2025
Recall History
No Recall HistoryView Full Drug Page
BRUKINSA — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.