IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 074916

Active Ingredient(s):
IBUPROFEN

Company:
ACTAVIS MID ATLANTIC

Original Approval or Tentative Approval Date:
December 12, 1999

Products on Application NDA 074916:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	100MG/5ML	SUSPENSION; ORAL	OTC	none

Recall Notices

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January 2009

IBUPROFEN Detail

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