Drug History: DEPAKOTE

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:	DEPAKOTE
FDA Application No:	(NDA) 018723
Active Ingredient(s):	DIVALPROEX SODIUM
Company:	ABBOTT

Label History

View the label approved on October 18, 2006 for DEPAKOTE, (NDA) 018723

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
10/13/2006	033	Labeling Revision	Letter Label
1/11/2006	032	Labeling Revision	Letter Label
12/9/2002	031	Control Supplement
11/5/2002	030	Control Supplement
12/12/2002	029	Labeling Revision	Letter
6/19/2000	028	Labeling Revision
9/22/1998	027	Control Supplement
4/2/1998	026	Manufacturing Change or Addition
5/8/1998	025	Package Change
12/24/1997	024	Formulation Revision
12/2/1996	022	Control Supplement
6/20/1996	020	New or Modified Indication
3/23/1995	019	Control Supplement
3/18/1996	017	New or Modified Indication
6/22/1994	015	Control Supplement
3/18/1994	013	Manufacturing Change or Addition
8/16/1989	012	Manufacturing Change or Addition
3/21/1989	011	Expiration Date Change
8/17/1988	009	Control Supplement
11/24/1986	008	Expiration Date Change
12/23/1985	005	Expiration Date Change
8/11/1986	004	Labeling Revision
12/6/1985	003	Control Supplement
8/11/1986	002	Labeling Revision
10/26/1984	001	Formulation Revision
3/10/1983	000	Approval

There are no Therapeutic Equivalents