NDC 70710-1650
Sugammadex 200 mg per 2 mL injection, solution
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Vadodara, India | Makes it and tests it | Serious problems, FDA actionApr 23, 2024 · 2 inspections, 1 with FDA action |
Product details
- Generic drug
- Sugammadex: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 200 mg per 2 mL
- Approval
- ANDA ANDA214290
- On the market since
- Jul 2, 2026
- Package NDCs
70710-1650-170710-1650-6- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2026
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