FEXOFENADINE HYDROCHLORIDE Detail

Drug Name(s):
FEXOFENADINE HYDROCHLORIDE

FDA Application No.:
NDA 076502

Active Ingredient(s):
FEXOFENADINE HYDROCHLORIDE

Company:
DR REDDYS LABS LTD

Original Approval or Tentative Approval Date:
April 11, 2006

Products on Application NDA 076502:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FEXOFENADINE HYDROCHLORIDE	180MG	TABLET; ORAL	Prescription	AB
FEXOFENADINE HYDROCHLORIDE	30MG	TABLET; ORAL	Prescription	AB

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last updated on 11-19-2008

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