Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Onesource Specialty Pharma Limited | Bengaluru, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJun 30, 2026 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Sugammadex: every company that makes it
- Form
- solution, intravenous
- Strength
- 200 mg per 2 mL
- Approval
- ANDA ANDA218814
- On the market since
- Jul 28, 2026
- Package NDCs
42023-830-10- Official label
- DailyMed (National Library of Medicine), updated Jul 28, 2026
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