IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 076359

Active Ingredient(s):
IBUPROFEN

Company:
PERRIGO

Original Approval or Tentative Approval Date:
January 15, 2004

Products on Application NDA 076359:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	100MG	TABLET, CHEWABLE; ORAL	OTC	none

Recall Notices

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January 2009

IBUPROFEN Detail

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