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Vecuronium Bromide for Injection - 41616-932-44 - (Vecuronium Bromide for Injection)

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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

Complete Information of Vecuronium Bromide for Injection


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