Drug History: DEPO-PROVERA

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:	DEPO-PROVERA
FDA Application No:	(NDA) 020246
Active Ingredient(s):	MEDROXYPROGESTERONE ACETATE
Company:	PHARMACIA AND UPJOHN

Label History

View the label approved on December 3, 2004 for DEPOPROVERA, (NDA) 020246

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
11/17/2004	025	Labeling Revision	Letter Label
5/23/2003	019	Control Supplement	Letter Label
5/23/2002	018	Control Supplement
4/26/2002	017	Control Supplement
6/7/2001	015	Manufacturing Change or Addition
4/3/2000	014	Manufacturing Change or Addition
10/28/2005	013	Labeling Revision	Letter Label
8/12/1998	012	Labeling Revision
1/31/1997	011	Labeling Revision
3/20/1996	009	Labeling Revision
11/28/1995	008	Control Supplement
5/3/1995	007	Control Supplement
2/1/1996	006	Control Supplement
12/1/1994	004	Labeling Revision
12/1/1994	003	Labeling Revision
2/17/1994	002	Manufacturing Change or Addition
10/29/1992	000	Approval

Therapeutic Equivalents