NDC 0944-2850
Cuvitru 200 mg per 1 mL injection, solution
On the label: Takeda Pharmaceuticals America, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxalta Belgium Manufacturing SA | Lessines, Belgium | Makes it | Problems found, fixed voluntarilyJun 18, 2013 · 1 inspection |
Product details
- Generic drug
- Human Immunoglobulin G: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 200 mg per 1 mL
- Approval
- BLA BLA125596
- On the market since
- Oct 18, 2016
- Package NDCs
0944-2850-010944-2850-020944-2850-030944-2850-040944-2850-050944-2850-060944-2850-070944-2850-080944-2850-090944-2850-10- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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