Product NDC: | 55154-0457 |
Proprietary Name: | vecuronium bromide |
Non Proprietary Name: | vecuronium bromide |
Active Ingredient(s): | 10 mg/10mL & nbsp; vecuronium bromide |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-0457 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074688 |
Marketing Category: | ANDA |
Start Marketing Date: | 19990825 |
Package NDC: | 55154-0457-5 |
Package Description: | 5 VIAL in 1 BAG (55154-0457-5) > 10 mL in 1 VIAL |
NDC Code | 55154-0457-5 |
Proprietary Name | vecuronium bromide |
Package Description | 5 VIAL in 1 BAG (55154-0457-5) > 10 mL in 1 VIAL |
Product NDC | 55154-0457 |
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 | 19990825 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | VECURONIUM BROMIDE |
Strength Number | 10 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Neuromuscular Nondepolarizing Blockade [PE],Nondepolarizing Neuromuscular Blocker [EPC] |