Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Catalent Pharma Solutions, LLC | Winchester, KY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 22, 2025 · 10 inspections |
| Changzhou SynTheAll Pharmaceutical Co., Ltd. | Changzhou, China | Makes the active ingredient and tests it | No problems foundMar 7, 2025 · 2 inspections |
| Siegfried Evionnaz SA | Evionnaz, Switzerland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyMar 31, 2023 · 6 inspections |
| Allpack Group AG | Reinach, Switzerland | Packages it and labels it | Problems found, fixed voluntarilyApr 28, 2023 · 6 inspections |
| AndersonBrecon Inc. | Rockford, IL, United States | Packages it and labels it | No problems foundAug 19, 2026 · 11 inspections |
| BeOne Pharmaceutical (Suzhou) Co.,Ltd | Suzhou, China | Tests it | Problems found, fixed voluntarilyJun 16, 2023 · 1 inspection |
| Sharp Packaging Services, LLC | Macungie, PA, United States | Packages it and labels it | Problems found, fixed voluntarilySep 12, 2025 · 6 inspections |
Product details
- Generic drug
- Zanubrutinib: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 160 mg
- Approval
- NDA NDA218785
- On the market since
- Aug 18, 2025
- Package NDCs
72579-122-01- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2026
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