IBU Detail

Drug Name(s):
IBU

FDA Application No.:
NDA 070083

Active Ingredient(s):
IBUPROFEN

Company:
BASF

Original Approval or Tentative Approval Date:
February 21, 1985

Products on Application NDA 070083:

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

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last updated on 01-08-2009

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