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Vecuronium Bromide
Vecuronium Bromide - 0409-1632-49 - (Vecuronium Bromide)
Drug Information of Vecuronium Bromide
| Product NDC: | 0409-1632 |
| Proprietary Name: | Vecuronium Bromide |
| Non Proprietary Name: | Vecuronium Bromide |
| Active Ingredient(s): | 1 mg/mL & 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 Bromide
| Product NDC: | 0409-1632 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075164 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19991021 |
Package Information of Vecuronium Bromide
| Package NDC: | 0409-1632-49 |
| Package Description: | 10 VIAL in 1 CARTON (0409-1632-49) > 10 mL in 1 VIAL |
NDC Information of Vecuronium Bromide
| NDC Code | 0409-1632-49 |
| Proprietary Name | Vecuronium Bromide |
| Package Description | 10 VIAL in 1 CARTON (0409-1632-49) > 10 mL in 1 VIAL |
| Product NDC | 0409-1632 |
| 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 | 19991021 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | VECURONIUM BROMIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |
