IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 072169

Active Ingredient(s):
IBUPROFEN

Company:
SANDOZ

Original Approval or Tentative Approval Date:
April 6, 1988

Products on Application NDA 072169:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	800MG	TABLET; ORAL	Prescription	AB

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last updated on 01-07-2009

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