Ethosuximide

NDC 69452-152 · Bionpharma Inc.

Generic nameEthosuximide

Dosage formCAPSULE, LIQUID FILLED

RouteORAL

Active ingredient(s)ETHOSUXIMIDE

Strength250 mg/1

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

Marketing categoryANDA

Packages

69452-152-20 — 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-152-20)

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, 62135-064 — Ethosuximide, 62135-790 — ETHOSUXIMIDE, 63629-8005 — Ethosuximide, 64380-878 — ETHOSUXIMIDE, 68999-064 — Ethosuximide

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