Ethosuximide

NDC 62135-064 · Chartwell RX, LLC

Generic nameEthosuximide

Dosage formSOLUTION

RouteORAL

Active ingredient(s)ETHOSUXIMIDE

Strength250 mg/5mL

Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Marketing categoryANDA

Packages

62135-064-47 — 473 mL in 1 BOTTLE (62135-064-47)

FDA lists these products with the same active ingredient.

0071-0237 — Ethosuximide, 0071-2418 — Ethosuximide, 0121-0670 — ETHOSUXIMIDE, 42806-708 — Ethosuximide, 42806-711 — Ethosuximide, 59762-2350 — Ethosuximide, 62135-790 — ETHOSUXIMIDE, 63629-8005 — Ethosuximide, 64380-878 — ETHOSUXIMIDE, 68999-064 — Ethosuximide, 69452-152 — Ethosuximide

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