Brukinsa
zanubrutinib · Capsule · Oral
No FDA structured label text is available for Brukinsa. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Zanubrutinib in 2 products
Brukinsa NDC products (2)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 72579-011 | Zanubrutinib 80 mg/1 Capsule | BeOne Medicines USA, Inc. | NDA |
| 72579-122 | Zanubrutinib 160 mg/1 Tablet, Film Coated | BeOne Medicines USA, Inc. | NDA |
Frequently asked questions
Who makes Brukinsa?
Brukinsa is listed by 1 labeler in the FDA NDC directory, including BeOne Medicines USA, Inc..