IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 071145

Active Ingredient(s):
IBUPROFEN

Company:
IVAX PHARMS

Original Approval or Tentative Approval Date:
September 22, 1986

Products on Application NDA 071145:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	400MG	TABLET; ORAL	Discontinued	none

Recall Notices

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January 2009

IBUPROFEN Detail

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