Composition
- Active ingredients
- ROCURONIUM BROMIDE 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ROCURONIUM BROMIDE 100MG/10ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA020214-003 · Discontinued
- ROCURONIUM BROMIDE 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableThis page
- ROCURONIUM BROMIDE 10MG/ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA020214-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA020214.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Zemuron
- Active substance
- rocuronium bromide
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Organon USA Inc
- Status
- Discontinued
- FDA approval
- 17 Mar 1994
- Application
- NDA020214-001