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) 018082
Active Ingredient(s):	VALPROIC ACID
Company:	ABBOTT

Label History

View the label approved on October 18, 2006 for DEPAKENE, (NDA) 018082

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	027	Labeling Revision	Letter Label
1/11/2006	026	Labeling Revision	Letter Label
12/12/2002	024	Labeling Revision	Letter
6/19/2000	023	Labeling Revision
5/16/2000	022	Labeling Revision
12/2/1996	021	Control Supplement
3/23/1995	018	Control Supplement
8/11/1986	013	Labeling Revision
12/4/1985	012	Labeling Revision
9/30/1982	007	Package Change
11/4/1981	006	Labeling Revision
12/9/1981	004	Labeling Revision
9/29/1980	003	Expiration Date Change
12/20/1979	002	Control Supplement
5/3/1979	001	Labeling Revision
2/28/1978	000	Approval

Therapeutic Equivalents