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Rocuronium
Rocuronium - 63323-426-05 - (ROCURONIUM BROMIDE)
Drug Information of Rocuronium
| Product NDC: | 63323-426 |
| Proprietary Name: | Rocuronium |
| 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
| Product NDC: | 63323-426 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078651 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091213 |
Package Information of Rocuronium
| Package NDC: | 63323-426-05 |
| Package Description: | 10 VIAL in 1 TRAY (63323-426-05) > 5 mL in 1 VIAL |
NDC Information of Rocuronium
| NDC Code | 63323-426-05 |
| Proprietary Name | Rocuronium |
| Package Description | 10 VIAL in 1 TRAY (63323-426-05) > 5 mL in 1 VIAL |
| Product NDC | 63323-426 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ROCURONIUM BROMIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091213 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | ROCURONIUM BROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |
