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rocuronium bromide
rocuronium bromide - 39822-4200-2 - (rocuronium bromide)
Drug Information of rocuronium bromide
| Product NDC: | 39822-4200 |
| 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): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of rocuronium bromide
| Product NDC: | 39822-4200 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091115 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121201 |
Package Information of rocuronium bromide
| Package NDC: | 39822-4200-2 |
| Package Description: | 10 VIAL in 1 CARTON (39822-4200-2) > 5 mL in 1 VIAL (39822-4200-1) |
NDC Information of rocuronium bromide
| NDC Code | 39822-4200-2 |
| Proprietary Name | rocuronium bromide |
| Package Description | 10 VIAL in 1 CARTON (39822-4200-2) > 5 mL in 1 VIAL (39822-4200-1) |
| Product NDC | 39822-4200 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | rocuronium bromide |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20121201 |
| Marketing Category Name | ANDA |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | ROCURONIUM BROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |
