Drug History: DEPAKENE

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:	DEPAKENE
FDA Application No:	(NDA) 018081
Active Ingredient(s):	VALPROIC ACID
Company:	ABBOTT

Label History

View the label approved on October 18, 2006 for DEPAKENE, (NDA) 018081

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	044	Labeling Revision	Letter Label
1/11/2006	042	Labeling Revision	Letter Label
12/12/2002	038	Labeling Revision	Letter
6/20/2000	036	Control Supplement
12/20/2000	035	Manufacturing Change or Addition
6/20/2000	034	Control Supplement
12/6/1999	033	Control Supplement
6/19/2000	032	Labeling Revision
9/22/1998	031	Manufacturing Change or Addition
5/8/1998	030	Package Change
5/16/2000	029	Labeling Revision
12/2/1996	028	Control Supplement
3/23/1995	025	Control Supplement
3/21/1989	021	Manufacturing Change or Addition
12/2/1987	020	Manufacturing Change or Addition
8/11/1986	018	Labeling Revision
5/30/1986	017	Labeling Revision
12/4/1985	016	Labeling Revision
5/30/1986	015	Labeling Revision
10/28/1983	014	Manufacturing Change or Addition
9/30/1982	012	Expiration Date Change
12/9/1981	008	Labeling Revision
11/4/1981	007	Labeling Revision
12/9/1981	005	Labeling Revision
6/16/1980	004	Expiration Date Change
12/20/1979	003	Formulation Revision
12/20/1979	002	Control Supplement
5/3/1979	001	Labeling Revision
2/28/1978	000	Approval

Therapeutic Equivalents