Visitor Monitoring Drug History: DEPAKOTE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: DEPAKOTE
FDA Application No: (NDA) 019680
Active Ingredient(s): DIVALPROEX SODIUM
Company: ABBOTT
 
Label History
 
View the label approved on October 18, 2006 for DEPAKOTE, (NDA) 019680


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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/13/2006 022Labeling Revision Letter
Label 
12/19/2006 021Labeling Revision Letter
Label 
1/11/2006 019Labeling Revision Letter
Label 
11/5/2002 016Control Supplement  
12/12/2002 015Labeling Revision Letter 
6/19/2000 014Labeling Revision  
5/8/1998 013Package Change  
12/2/1996 011Control Supplement  
4/26/1996 010Labeling Revision  
6/20/1996 008New or Modified Indication  
3/23/1995 007Control Supplement  
1/14/1993 002Control Supplement  
9/12/1989 000Approval  
 
There are no Therapeutic Equivalents
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