Drug Details: DEPAKOTE CP

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	DEPAKOTE CP
FDA Application No:	(NDA) 019794
Active Ingredient(s):	DIVALPROEX SODIUM
Company:	ABBOTT
Original Approval or Tentative Approval Date:	July 11, 1990
Chemical Type:	3 New dosage form
Review Classification:	S Standard review drug

There are no Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

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Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
DEPAKOTE CP	DIVALPROEX SODIUM	EQ 250MG BASE	TABLET, DELAYED RELEASE; ORAL	Discontinued	No	None
DEPAKOTE CP	DIVALPROEX SODIUM	EQ 500MG BASE	TABLET, DELAYED RELEASE; ORAL	Discontinued	No	None

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