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) 019716
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	SCHERING

Label History

View the label approved on August 28, 2006 for DIPROLENE, (NDA) 019716

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	022	Patient Population Altered	Letter Label
4/24/2006	021	Labeling Revision	Letter
5/11/2001	012	Control Supplement
9/7/2000	011	Package Change
5/14/1999	010	Control Supplement
7/31/1998	009	Control Supplement
6/15/1998	008	Control Supplement
1/25/1996	007	Manufacturing Change or Addition
10/7/2005	006	Labeling Revision	Letter Label
7/1/1992	005	Package Change
8/1/1990	004	Control Supplement
5/24/1989	003	Labeling Revision
4/6/1989	002	Package Change
8/1/1988	000	Approval

Therapeutic Equivalents