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Valproate Sodium

NDC 0143-9637 · Hikma Pharmaceuticals USA Inc.

Generic nameValproate Sodium
Dosage formINJECTION
RouteINTRAVENOUS
Active ingredient(s)VALPROATE SODIUM
Strength100 mg/mL
Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
Marketing categoryANDA

Packages

0143-9637-10 — 10 VIAL, SINGLE-DOSE in 1 TRAY (0143-9637-10) / 5 mL in 1 VIAL, SINGLE-DOSE (0143-9637-01)

Billed under HCPCS

J3379 — Injection, valproate sodium, 5 mg Medicare Part B payment limit (ASP + 6%): $0.01

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 37662-0730 — 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.