Drug History: DIPROLENE

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
FDA Application No:	(NDA) 018741
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	SCHERING

Label History

View the label approved on August 29, 2006 for DIPROLENE, (NDA) 018741

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	028	Patient Population Altered	Letter Label
11/10/1998	021	Package Change
6/15/1998	020	Control Supplement
7/31/1998	019	Control Supplement
6/15/1998	018	Control Supplement
11/30/1995	017	Control Supplement
10/7/2005	016	Labeling Revision	Letter Letter Label Label
2/9/2006	016	Labeling Revision	Letter Letter Label Label
11/8/1991	015	Control Supplement
8/1/1990	014	Control Supplement
5/24/1989	013	Labeling Revision
11/30/1988	012	Package Change
10/29/1987	009	Manufacturing Change or Addition
9/12/1986	008	Manufacturing Change or Addition
5/20/1986	007	Control Supplement
4/23/1986	005	Manufacturing Change or Addition
2/22/1985	004	Package Change
11/16/1984	003	Labeling Revision
12/15/1983	002	Labeling Revision
9/29/1986	001	Labeling Revision
7/27/1983	000	Approval

Therapeutic Equivalents