Rocuronium Bromide 71839-0141
Product NDC
71839-0141- Manufacturer
- Be Pharmaceuticals Inc.
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 12, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA216234
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Rocuronium Bromide | 10 mg/mL |
Drug Class
Neuromuscular Nondepolarizing Blockade [PE]Nondepolarizing Neuromuscular Blocker [EPC]
Packaging Options(1)
10 VIAL, MULTI-DOSE in 1 CARTON (71839-141-10) / 5 mL in 1 VIAL, MULTI-DOSE (71839-141-01)