NDC 70069-836
Bortezomib 3.5 mg per 3.5 mL injection, powder, lyophilized, for solution
On the label: Somerset Therapeutics, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Reliance Life Sciences Private Limited | Navi Mumbai, India | Makes it, makes the active ingredient, tests it, packages it and labels it | Serious problems, FDA actionFeb 27, 2026 · 8 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 per 3.5 mL
- Approval
- ANDA ANDA211898
- On the market since
- Apr 29, 2025
- Package NDCs
70069-836-01- Official label
- DailyMed (National Library of Medicine), updated May 10, 2025
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