Zonisamide

NDC 62756-260 · Sun Pharmaceutical Industries, Inc.

Generic nameZonisamide

Dosage formCAPSULE

RouteORAL

Active ingredient(s)ZONISAMIDE

Strength100 mg/1

Pharmacologic classAnti-epileptic Agent [EPC], Carbonic Anhydrase Inhibitors [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], P-Glycoprotein Inhibitors [MoA], Sulfonamides [CS]

Marketing categoryANDA

Packages

62756-260-01 — 30 CAPSULE in 1 BOTTLE (62756-260-01)

62756-260-03 — 100 CAPSULE in 1 BOTTLE (62756-260-03)

62756-260-04 — 1000 CAPSULE in 1 BOTTLE (62756-260-04)

62756-260-05 — 500 CAPSULE in 1 BOTTLE (62756-260-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50268-816 — Zonisamide, 52652-8001 — ZONISAMIDE, 59212-680 — Zonisamide, 59212-681 — Zonisamide, 59651-378 — Zonisamide, 59651-379 — Zonisamide, 59651-380 — Zonisamide, 60687-230 — Zonisamide, 62756-258 — Zonisamide, 62756-259 — Zonisamide, 63187-583 — Zonisamide, 63187-897 — Zonisamide, 63629-3293 — Zonisamide, 68001-242 — Zonisamide, 68001-243 — Zonisamide, 68001-244 — Zonisamide, 68462-128 — Zonisamide, 68462-129 — Zonisamide, 68462-130 — Zonisamide, 68788-4004 — Zonisamide, +30 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.