FENOFIBRATE (MICRONIZED) Detail

Drug Name(s):
FENOFIBRATE (MICRONIZED)

FDA Application No.:
NDA 075868

Active Ingredient(s):
FENOFIBRATE

Company:
IMPAX LABS

Original Approval or Tentative Approval Date:
October 26, 2003

Products on Application NDA 075868:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENOFIBRATE	134MG	CAPSULE; ORAL	Prescription	AB

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January 2009

FENOFIBRATE (MICRONIZED) Detail

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