IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 072096

Active Ingredient(s):
IBUPROFEN

Company:
PERRIGO

Original Approval or Tentative Approval Date:
March 27, 1989

Products on Application NDA 072096:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	200MG	TABLET; ORAL	OTC	none

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last updated on 01-07-2009

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