IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 071639

Active Ingredient(s):
IBUPROFEN

Company:
VINTAGE PHARMS

Original Approval or Tentative Approval Date:
February 1, 1988

Products on Application NDA 071639:

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

Recall Notices

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KRC Food Trading Inc. Recall of Fish Cake Sushi (December 23)

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January 2009

IBUPROFEN Detail

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