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Vecuronium Bromide - 0409-1632-49 - (Vecuronium Bromide)

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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]

Complete Information of Vecuronium Bromide


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