NDC 43598-924
Sugammadex 200 mg per 2 mL injection, solution
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 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 ANDA214236
- On the market since
- Jul 28, 2026
- Package NDCs
43598-924-1143598-924-26- Official label
- DailyMed (National Library of Medicine), updated Feb 18, 2026
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