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Rocuronium Bromide
Rocuronium Bromide - 0781-3220-70 - (Rocuronium Bromide)
Drug Information of Rocuronium Bromide
| Product NDC: | 0781-3220 |
| Proprietary Name: | Rocuronium Bromide |
| Non Proprietary Name: | Rocuronium Bromide |
| Active Ingredient(s): | 10 mg/mL & nbsp; Rocuronium Bromide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rocuronium Bromide
| Product NDC: | 0781-3220 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079195 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081205 |
Package Information of Rocuronium Bromide
| Package NDC: | 0781-3220-70 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3220-70) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Rocuronium Bromide
| NDC Code | 0781-3220-70 |
| Proprietary Name | Rocuronium Bromide |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3220-70) > 10 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0781-3220 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rocuronium Bromide |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20081205 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | ROCURONIUM BROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |
