FdaApplication
NDA 217472
Identifiers
- fda_app_no: NDA217472
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | NDA |
| approval_date | 2025-06-09 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ROCURONIUM BROMIDE | ROCURONIUM BROMIDE | 50MG/5ML (10MG/ML) | SOLUTION;INTRAVENOUS |
| ROCURONIUM BROMIDE | ROCURONIUM BROMIDE | 100MG/10ML (10MG/ML) | SOLUTION;INTRAVENOUS |
2 products