Product NDC: | 55390-037 |
Proprietary Name: | Vecuronium Bromide |
Non Proprietary Name: | Vecuronium Bromide |
Active Ingredient(s): | 5 mg/mL & nbsp; Vecuronium Bromide |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55390-037 |
Labeler Name: | Bedford Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075549 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000801 |
Package NDC: | 55390-037-10 |
Package Description: | 10 VIAL in 1 BOX (55390-037-10) > 10 mL in 1 VIAL |
NDC Code | 55390-037-10 |
Proprietary Name | Vecuronium Bromide |
Package Description | 10 VIAL in 1 BOX (55390-037-10) > 10 mL in 1 VIAL |
Product NDC | 55390-037 |
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 | 20000801 |
Marketing Category Name | ANDA |
Labeler Name | Bedford Laboratories |
Substance Name | VECURONIUM BROMIDE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes |