IBUPROHM COLD AND SINUS Detail

Drug Name(s):
IBUPROHM COLD AND SINUS

FDA Application No.:
NDA 074567

Active Ingredient(s):
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE

Company:
OHM LABS

Original Approval or Tentative Approval Date:
January 27, 2002

Products on Application NDA 074567:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE	200MG;30MG	TABLET; ORAL	OTC	none

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January 2009

IBUPROHM COLD AND SINUS Detail

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