IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 070437

Active Ingredient(s):
IBUPROFEN

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
August 20, 1985

Products on Application NDA 070437:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	600MG	TABLET; ORAL	Prescription	AB

Recall Notices

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January 2009

IBUPROFEN Detail

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