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Divalproex Sodium

NDC 37662-0730 · Hahnemann Laboratories, INC.

Generic nameDivalproex Sodium
Dosage formPELLET
RouteORAL
Active ingredient(s)VALPROATE SODIUM
Strength500 [hp_C]/1
Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

37662-0730-1 — 200 PELLET in 1 VIAL, GLASS (37662-0730-1)

37662-0730-2 — 500 PELLET in 1 VIAL, GLASS (37662-0730-2)

37662-0730-3 — 3000 PELLET in 1 BOTTLE, GLASS (37662-0730-3)

37662-0730-4 — 10000 PELLET in 1 BOTTLE, GLASS (37662-0730-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0143-9637 — Valproate Sodium, 0143-9785 — Valproate Sodium, 25021-797 — Valproate Sodium, 37662-0725 — Divalproex Sodium, 37662-0726 — Divalproex Sodium, 37662-0727 — Divalproex Sodium, 37662-0728 — Divalproex Sodium, 37662-0729 — Divalproex Sodium, 37662-0731 — Divalproex Sodium, 37662-0732 — Divalproex Sodium, 37662-2862 — Divalproex Sodium, 37662-2863 — Divalproex Sodium, 37662-2864 — Divalproex Sodium, 37662-2865 — Divalproex Sodium, 37662-2866 — Divalproex Sodium, 37662-2867 — Divalproex Sodium, 37662-2868 — Divalproex Sodium, 37662-2869 — Divalproex Sodium, 63323-494 — VALPROATE SODIUM

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.