IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 070908

Active Ingredient(s):
IBUPROFEN

Company:
MUTUAL PHARM

Original Approval or Tentative Approval Date:
December 16, 1986

Products on Application NDA 070908:

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

Recall Notices

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FDA Announces Class I Recall of Ophthalmic Surgical Device
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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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