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 |
| Sanofi-Aventis Deutschland GmbH | Frankfurt am Main, Germany | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 25, 2022 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Aflibercept: every company that makes it
- Form
- solution, concentrate, intravenous
- Strength
- 200 mg per 8 mL
- Approval
- BLA BLA125418
- On the market since
- Aug 3, 2012
- Package NDCs
0024-5841-01- Official label
- DailyMed (National Library of Medicine), updated Oct 6, 2025
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