BRUKINSA 80 mg/1
zanubrutinib · CAPSULE · BeOne Medicines USA, Inc.
No Recall History
Plain English
BRUKINSA is a capsule containing zanubrutinib at 80 mg/1, taken oral. Manufactured by BeOne Medicines USA, Inc..
Key Facts
- Brand Name
- BRUKINSA
- Generic Name
- zanubrutinib
- NDC Code (Product)
72579-011- Manufacturer
- BeOne Medicines USA, Inc.
- Strength
- 80 mg/1
- Dosage Form
- CAPSULE
- Route
- ORAL
- Marketing Status
- Application #
- NDA213217
- Drug Class
- Kinase Inhibitor [EPC]
- Marketing Start
- 11/14/2019
Recall History
No Recall HistoryFrequently Asked Questions
What is BRUKINSA used for?
BRUKINSA contains zanubrutinib. It is a capsule taken oral. Consult your doctor for specific uses.
Is BRUKINSA a controlled substance?
BRUKINSA is not classified as a controlled substance by the DEA.
What is the generic name for BRUKINSA?
The generic name for BRUKINSA is zanubrutinib. There are no other listed brand versions of zanubrutinib.
What is the NDC code for BRUKINSA 80 mg/1?
The NDC (National Drug Code) for BRUKINSA 80 mg/1 is 72579-011, listed by BeOne Medicines USA, Inc..
Other BRUKINSA Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)