Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Regeneron Pharmaceuticals, Inc. | Rensselaer, NY, United States | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyMar 22, 2024 · 10 inspections |
| Sanofi Winthrop Industrie | Le Trait, France | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 25, 2023 · 6 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 |
| Genzyme Corporation | Northborough, MA, United States | Packages it and labels it | No problems foundAug 14, 2025 · 6 inspections |
Product details
- Generic drug
- Sarilumab: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 200 mg per 1.14 mL
- Approval
- BLA BLA761037
- On the market since
- May 22, 2017
- Package NDCs
0024-5922-000024-5922-010024-5922-02- Official label
- DailyMed (National Library of Medicine), updated Feb 27, 2026
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