Drug History: DIPROSONE

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:	DIPROSONE
FDA Application No:	(NDA) 017781
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	SCHERING

Label History

View the label approved on October 3, 2001 for DIPROSONE, (NDA) 017781

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
5/11/2001	023	Control Supplement
10/3/2001	022	Patient Population Altered	Letter Label Review
9/7/2000	021	Package Change
5/14/1999	020	Control Supplement
6/15/1998	019	Control Supplement
7/31/1998	018	Control Supplement
6/15/1998	017	Control Supplement
11/21/1997	016	Formulation Revision
10/3/2001	015	Labeling Revision	Letter Label Review
8/8/1995	014	Package Change
8/1/1990	013	Control Supplement
4/6/1989	012	Package Change
5/20/1986	011	Control Supplement
6/29/1984	010	Control Supplement
12/2/1982	009	Final Printed Labeling - MarkIV
4/19/1982	008	Manufacturing Change or Addition
9/2/1981	007	Manufacturing Change or Addition
9/15/1981	006	Control Supplement
6/26/1980	004	Expiration Date Change
7/6/1979	003	Control Supplement
5/12/1980	002	Control Supplement
4/24/1980	001	Labeling Revision
2/1/1977	000	Approval

Therapeutic Equivalents