FEXOFENADINE HYDROCHLORIDE Detail

Drug Name(s):
FEXOFENADINE HYDROCHLORIDE

FDA Application No.:
NDA 076447

Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE

Company:
TEVA

Original Approval or Tentative Approval Date:
August 31, 2005

Products on Application NDA 076447:

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

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last updated on 12-05-2008