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Vecuronium
Vecuronium - 25021-658-20 - (vecuronium bromide)
Drug Information of Vecuronium
| Product NDC: | 25021-658 |
| Proprietary Name: | Vecuronium |
| Non Proprietary Name: | vecuronium bromide |
| Active Ingredient(s): | 20 mg/20mL & nbsp; vecuronium bromide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vecuronium
| Product NDC: | 25021-658 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078274 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110801 |
Package Information of Vecuronium
| Package NDC: | 25021-658-20 |
| Package Description: | 10 VIAL in 1 CARTON (25021-658-20) > 20 mL in 1 VIAL |
NDC Information of Vecuronium
| NDC Code | 25021-658-20 |
| Proprietary Name | Vecuronium |
| Package Description | 10 VIAL in 1 CARTON (25021-658-20) > 20 mL in 1 VIAL |
| Product NDC | 25021-658 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | vecuronium bromide |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110801 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | VECURONIUM BROMIDE |
| Strength Number | 20 |
| Strength Unit | mg/20mL |
| Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |
