Drug History: DEPAKOTE CP

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DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

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Label and Approval History

Drug Name:	DEPAKOTE CP
FDA Application No:	(NDA) 019794
Active Ingredient(s):	DIVALPROEX SODIUM
Company:	ABBOTT

Label History

Labels are not available on this site for DEPAKOTE CP, (NDA) 019794

Approval History

Action Date	Supplement Number	Approval Type	Letters, Reviews, Labels, Patient Package Insert
12/2/1996	002	Control Supplement
3/23/1995	001	Control Supplement
7/11/1990	000	Approval

There are no Therapeutic Equivalents

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