GEMFIBROZIL Detail

Drug Name(s):
GEMFIBROZIL

FDA Application No.:
NDA 074156

Active Ingredient(s):
GEMFIBROZIL

Company:
WATSON LABS

Products on Application NDA 074156:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GEMFIBROZIL	600MG	TABLET; ORAL	Discontinued	none

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last updated on 01-07-2009

GEMFIBROZIL Detail

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