GEMFIBROZIL Detail

Drug Name(s):
GEMFIBROZIL

FDA Application No.:
NDA 074256

Active Ingredient(s):
GEMFIBROZIL

Company:
TEVA

Original Approval or Tentative Approval Date:
February 27, 1996

Products on Application NDA 074256:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
GEMFIBROZIL	600MG	TABLET; ORAL	Prescription	AB

Recall Notices

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January 2009

GEMFIBROZIL Detail

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