FENOFIBRATE (MICRONIZED) Detail

Drug Name(s):
FENOFIBRATE (MICRONIZED)

FDA Application No.:
NDA 075753

Active Ingredient(s):
FENOFIBRATE

Company:
TEVA

Original Approval or Tentative Approval Date:
September 2, 2002

Products on Application NDA 075753:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FENOFIBRATE	200MG	CAPSULE; ORAL	Prescription	AB
FENOFIBRATE	67MG	CAPSULE; ORAL	Prescription	AB

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last updated on 12-05-2008