Drug History: DEPACON

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:	DEPACON
FDA Application No:	(NDA) 020593
Active Ingredient(s):	VALPROATE SODIUM
Company:	ABBOTT

Label History

View the label approved on October 18, 2006 for DEPACON, (NDA) 020593

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	015	Labeling Revision	Letter Label
1/11/2006	011	Labeling Revision	Letter Label
12/12/2002	009	Labeling Revision	Letter
8/12/2002	008	Control Supplement
6/26/2002	007	Control Supplement
1/24/2002	006	New Dosage Regimen	Letter Label
6/20/2000	005	Control Supplement
5/15/2000	004	Control Supplement
12/8/1999	003	Control Supplement
6/19/2000	002	Labeling Revision
12/16/1997	001	Control Supplement
12/30/1996	000	Approval

Therapeutic Equivalents