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) 017691
Active Ingredient(s):	BETAMETHASONE DIPROPIONATE
Company:	SCHERING

Label History

View the label approved on October 3, 2001 for DIPROSONE, (NDA) 017691

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
10/3/2001	024	Patient Population Altered	Letter Label Review
11/10/1998	023	Package Change
12/7/1998	022	Control Supplement
7/31/1998	021	Control Supplement
6/15/1998	020	Control Supplement
10/3/2001	019	Labeling Revision	Letter Label Review
7/5/1990	018	Control Supplement
8/1/1990	017	Control Supplement
9/12/1986	016	Manufacturing Change or Addition
5/20/1986	015	Control Supplement
6/1/1984	013	Package Change
3/1/1984	012	Package Change
4/19/1982	011	Manufacturing Change or Addition
7/21/1982	010	General Efficacy (MarkIV)
9/2/1981	009	Manufacturing Change or Addition
12/26/1979	007	Distributor
8/29/1979	006	Expiration Date Change
6/20/1979	005	Control Supplement
5/12/1980	004	Control Supplement
1/2/1979	003	Labeling Revision
9/6/1977	002	Package Change
6/8/1976	001	Labeling Revision
4/15/1976	000	Approval

Therapeutic Equivalents