NDC 0143-9098
bortezomib 3.5 mg injection, powder, lyophilized, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jiangsu Hansoh Pharmaceutical Group Co., Ltd. FDF site | Lianyungang, China | Makes it, tests it, packages it and labels it | Serious problems, FDA actionApr 24, 2026 · 2 inspections, 1 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 ANDA215011
- On the market since
- Jul 27, 2022
- Package NDCs
0143-9098-01- Official label
- DailyMed (National Library of Medicine), updated Nov 22, 2021
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