UTIMOX Detail

Drug Name(s):
UTIMOX

FDA Application No.:
NDA 062127

Active Ingredient(s):
AMOXICILLIN

Company:
PARKE DAVIS

Products on Application NDA 062127:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AMOXICILLIN	250MG/5ML	FOR SUSPENSION; ORAL	Discontinued	none

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last updated on 01-08-2009

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