FEXOFENADINE Detail

Drug Name(s):
FEXOFENADINE

FDA Application No.:
NDA 077081

Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE

Company:
MYLAN PHARMA

Products on Application NDA 077081:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FEXOFENADINE HYDROCHLORIDE	180MG	TABLET; ORAL	Tentative approval	none
FEXOFENADINE HYDROCHLORIDE	30MG	TABLET; ORAL	Tentative approval	none

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last updated on 12-05-2008