Drug History: FLOVENT

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:	FLOVENT
FDA Application No:	(NDA) 020548
Active Ingredient(s):	FLUTICASONE PROPIONATE
Company:	GLAXOSMITHKLINE

Label History

View the label approved on April 5, 2004 for FLOVENT, (NDA) 020548

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
3/26/2004	020	Labeling Revision	Letter Label
10/8/2003	019	Labeling Revision	Letter Label
6/20/2003	016	Labeling Revision	Letter Label
8/15/2001	014	Manufacturing Change or Addition
5/17/2000	012	Control Supplement
12/22/1998	008	Labeling Revision	Review
11/4/1998	007	Control Supplement
7/31/1998	006	Control Supplement
4/13/1998	005	Manufacturing Change or Addition
2/18/1998	004	Control Supplement
10/14/1997	003	Labeling Revision
6/5/1996	002	Control Supplement
5/7/1996	001	Control Supplement
3/27/1996	000	Approval

Therapeutic Equivalents