FEXOFENADINE HYDROCHLORIDE Detail

Drug Name(s):
FEXOFENADINE HYDROCHLORIDE

FDA Application No.:
NDA 076169

Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE

Company:
BARR

Original Approval or Tentative Approval Date:
July 12, 2005

Products on Application NDA 076169:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FEXOFENADINE HYDROCHLORIDE	60MG	CAPSULE; ORAL	Prescription	AB

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January 2009

FEXOFENADINE HYDROCHLORIDE Detail

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