IBUPROFEN Detail

Drug Name(s):
IBUPROFEN

FDA Application No.:
NDA 074978

Active Ingredient(s):
IBUPROFEN

Company:
ACTAVIS MID ATLANTIC

Original Approval or Tentative Approval Date:
March 24, 1998

Products on Application NDA 074978:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN	100MG/5ML	SUSPENSION; ORAL	Prescription	AB

Recall Notices

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January 2009

IBUPROFEN Detail

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