NDC 68001-540
Bortezomib 3.5 mg injection, powder, lyophilized, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Qilu Pharmaceutical (Hainan) Co., Ltd. | Haikou, China | Makes it and tests it | Problems found, fixed voluntarilyMay 19, 2023 · 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 ANDA210824
- On the market since
- May 16, 2022
- Package NDCs
68001-540-36- Official label
- DailyMed (National Library of Medicine), updated May 16, 2022
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