FdaApplication
NDA 020214
Identifiers
- fda_app_no: NDA020214
Properties
| Property | Value |
|---|---|
| applicant_name | ORGANON USA INC |
| application_type | NDA |
| approval_date | 1994-03-17 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZEMURON | ROCURONIUM BROMIDE | 100MG/10ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| ZEMURON | ROCURONIUM BROMIDE | 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| ZEMURON | ROCURONIUM BROMIDE | 10MG/ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
3 products