NDC 61755-014
Veopoz 200 mg per 1 mL injection, solution
On the label: Regeneron Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Regeneron Pharmaceuticals, Inc. | Rensselaer, NY, United States | Makes the active ingredient and tests it | Problems found, fixed voluntarilyMar 22, 2024 · 10 inspections |
Product details
- Generic drug
- Pozelimab: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 200 mg per 1 mL
- Approval
- BLA BLA761339
- On the market since
- Aug 18, 2023
- Package NDCs
61755-014-0061755-014-01- Official label
- DailyMed (National Library of Medicine), updated Dec 4, 2025
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