Last Updated: June 24, 2026

Details for New Drug Application (NDA): 211505

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NDA 211505 describes DIVALPROEX SODIUM, which is a drug marketed by Ajanta Pharma Ltd, Alembic, Dr Reddys Labs Ltd, Mankind Pharma, Rising, Teva Pharms Usa, Zydus Pharms Usa Inc, Actavis Labs Fl Inc, Apotex, Aurobindo Pharma Ltd, Chartwell Rx, Invatech, Lupin, Mylan, Orbion Pharms, Ph Health, Pharmobedient, Prinston Inc, Sun Pharm Inds, Teva, Unichem Labs Ltd, Upsher Smith Labs, Amneal Pharms, Annora Pharma, Cosette, Impax Labs, Reddys, Sciegen Pharms, Unichem, and Yichang Humanwell, and is included in thirty-eight NDAs. It is available from forty-four suppliers. Additional details are available on the DIVALPROEX SODIUM profile page.

The generic ingredient in DIVALPROEX SODIUM is divalproex sodium. There are eighteen drug master file entries for this compound. Forty-five suppliers are listed for this compound. Additional details are available on the divalproex sodium profile page.

Summary for 211505

Tradename:	DIVALPROEX SODIUM
Applicant:	Teva Pharms Usa
Ingredient:	divalproex sodium
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE, DELAYED REL PELLETS;ORAL			Strength	EQ 125MG VALPROIC ACID
Approval Date:	Nov 17, 2020	TE:		RLD:	No

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