Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| WuXi Biologics Co., Ltd. | Wuxi, China | Makes the active ingredient and tests it | Problems found, fixed voluntarilyJul 3, 2026 · 3 inspections |
| AndersonBrecon Inc. | Rockford, IL, United States | Packages it and labels it | No problems foundAug 19, 2026 · 11 inspections |
Product details
- Generic drug
- Pemivibart: every company that makes it
- Form
- injection, intravenous
- Strength
- 125 mg per 1 mL
- Approval
- Emergency Use Authorization EUA000122
- On the market since
- Mar 22, 2024
- Package NDCs
81960-031-03- Official label
- DailyMed (National Library of Medicine), updated Sep 12, 2025
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