Drug History: FLAREX

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9

Label and Approval History

Drug Name:	FLAREX
FDA Application No:	(NDA) 019079
Active Ingredient(s):	FLUOROMETHOLONE ACETATE
Company:	ALCON

Label History

View the label approved on November 9, 2006 for FLAREX, (NDA) 019079

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
11/8/2006	024	Labeling Revision	Letter Label
12/11/2002	023	Control Supplement
12/4/2002	022	Control Supplement
6/10/2002	021	Control Supplement
3/16/2001	020	Control Supplement
2/18/2000	018	Manufacturing Change or Addition
11/5/1999	017	Control Supplement
8/17/1999	016	Control Supplement
2/5/1999	015	Manufacturing Change or Addition
3/11/1999	014	Control Supplement
2/4/1999	013	Manufacturing Change or Addition
8/4/1998	012	Control Supplement
7/30/1997	011	Control Supplement
4/21/1997	010	Control Supplement
9/26/1996	009	Labeling Revision
7/19/1996	008	Manufacturing Change or Addition
3/18/1996	007	Control Supplement
11/1/1995	006	Control Supplement
11/1/1995	005	Control Supplement
6/13/1995	004	Package Change
3/4/1987	003	Control Supplement
12/9/1986	002	Labeling Revision
3/24/1986	001	Formulation Revision
2/11/1986	000	Approval

There are no Therapeutic Equivalents