Drug application
SUGAMMADEX (SUGAMMADEX)
Drugs@FDA ANDA 213868 · FRESENIUS KABI USA LLC
Key facts
| Drug name | SUGAMMADEX |
|---|---|
| Active ingredients | SUGAMMADEX |
| Application type | ANDA |
| Application number | 213868 |
| Company | FRESENIUS KABI USA LLC |
| Dosage forms | INJECTION, SOLUTION |
| Strength | 100MG/1ML |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Nov 6, 2025 |
At a glance
- 1–9 Submissions
- None Label versions
- None Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.