Drug History: DIPROLENE AF

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:	DIPROLENE AF
FDA Application No:	(NDA) 019555
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	SCHERING

Label History

View the label approved on August 28, 2006 for DIPROLENE AF, (NDA) 019555

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
8/28/2006	026	Patient Population Altered	Letter Label
4/4/2001	017	Control Supplement
10/3/2001	016	Patient Population Altered	Letter Label Review
8/14/2000	015	Package Change
5/14/1999	014	Control Supplement
11/10/1998	013	Package Change
12/7/1998	012	Control Supplement
7/31/1998	011	Control Supplement
6/15/1998	010	Control Supplement
11/30/1995	009	Control Supplement
10/3/2001	008	Labeling Revision	Letter Label Review
6/29/1990	007	Control Supplement
8/1/1990	006	Control Supplement
5/24/1989	005	Labeling Revision
11/8/1988	004	Labeling Revision
10/29/1987	002	Manufacturing Change or Addition
4/27/1987	000	Approval

Therapeutic Equivalents