NDC 51817-586
Bortezomib 3.5 mg injection, powder, lyophilized, for solution
On the label: Pharmascience Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pharmascience Inc. | Candiac, Canada | Makes it | Problems found, fixed voluntarilyFeb 13, 2024 · 5 inspections |
Product details
- Generic drug
- Bortezomib: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 3.5 mg
- Approval
- ANDA ANDA208392
- On the market since
- May 2, 2022
- Package NDCs
51817-586-01- Official label
- DailyMed (National Library of Medicine), updated May 2, 2022
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