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Vecuronium Bromide for Injection
Vecuronium Bromide for Injection - 41616-932-44 - (Vecuronium Bromide for Injection)
Drug Information of Vecuronium Bromide for Injection
| Product NDC: | 41616-932 |
| Proprietary Name: | Vecuronium Bromide for Injection |
| Non Proprietary Name: | Vecuronium Bromide for Injection |
| Active Ingredient(s): | 1 mg/mL & nbsp; Vecuronium Bromide for Injection |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vecuronium Bromide for Injection
| Product NDC: | 41616-932 |
| Labeler Name: | SUN PHARMA GLOBAL INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079001 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090721 |
Package Information of Vecuronium Bromide for Injection
| Package NDC: | 41616-932-44 |
| Package Description: | 10 VIAL in 1 BOX (41616-932-44) > 20 mL in 1 VIAL (41616-932-40) |
NDC Information of Vecuronium Bromide for Injection
| NDC Code | 41616-932-44 |
| Proprietary Name | Vecuronium Bromide for Injection |
| Package Description | 10 VIAL in 1 BOX (41616-932-44) > 20 mL in 1 VIAL (41616-932-40) |
| Product NDC | 41616-932 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Vecuronium Bromide for Injection |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090721 |
| Marketing Category Name | ANDA |
| Labeler Name | SUN PHARMA GLOBAL INC. |
| Substance Name | VECURONIUM BROMIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
