LARGON Detail

Drug Name(s):
LARGON

FDA Application No.:
NDA 012382

Active Ingredient(s):
PROPIOMAZINE HYDROCHLORIDE

Company:
BAXTER HLTHCARE CORP

Products on Application NDA 012382:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PROPIOMAZINE HYDROCHLORIDE	20MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 11-21-2008

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