NDC 63323-821
Bortezomib 3.5 mg injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Bortezomib: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous; subcutaneous
- Strength
- 3.5 mg
- Approval
- ANDA ANDA209659
- On the market since
- May 2, 2022
- Package NDCs
63323-821-10- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?