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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 077615
Company: APOTEX

Products on ANDA 77615

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
DIVALPROEX SODIUM	DIVALPROEX SODIUM	EQ 500MG VALPROIC ACID	TABLET, DELAYED RELEASE;ORAL	Discontinued	None	No	No
DIVALPROEX SODIUM	DIVALPROEX SODIUM	EQ 250MG VALPROIC ACID	TABLET, DELAYED RELEASE;ORAL	Discontinued	None	No	No
DIVALPROEX SODIUM	DIVALPROEX SODIUM	EQ 125MG VALPROIC ACID	TABLET, DELAYED RELEASE;ORAL	Discontinued	None	No	No

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