IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 073019

Active Ingredient(s):
IBUPROFEN

Company:
MCNEIL

Original Approval or Tentative Approval Date:
March 29, 1994

Products on Application NDA 073019:

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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