Drug History: ALLEGRA

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	ALLEGRA
FDA Application No:	(NDA) 020625
Active Ingredient(s):	FEXOFENADINE HYDROCHLORIDE
Company:	SANOFI AVENTIS US

Label History

View the label approved on May 29, 2003 for ALLEGRA, (NDA) 020625

To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
5/12/2003	012	Efficacy Supplement with Clinical Data to Support	Letter Label
7/11/2001	011	Labeling Revision	Letter
5/12/2003	010	Efficacy Supplement with Clinical Data to Support	Letter Label
1/6/2000	009	Manufacturing Change or Addition
1/21/2000	008	Control Supplement
12/22/1998	007	Labeling Revision
7/6/1998	006	Manufacturing Change or Addition
1/29/1998	004	Control Supplement
1/28/1997	003	Manufacturing Change or Addition
10/16/1996	001	Package Change
7/25/1996	000	Approval	Label

Therapeutic Equivalents