IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 071769

Active Ingredient(s):
IBUPROFEN

Company:
IVAX PHARMS

Original Approval or Tentative Approval Date:
May 7, 1987

Products on Application NDA 071769:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	800MG	TABLET; ORAL	Discontinued	none

Recall Notices

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January 2009

IBUPROFEN Detail

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