Zonisamide

NDC 71335-9679 · Bryant Ranch Prepack

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

71335-9679-1 — 100 CAPSULE in 1 BOTTLE (71335-9679-1)

71335-9679-2 — 90 CAPSULE in 1 BOTTLE (71335-9679-2)

71335-9679-3 — 30 CAPSULE in 1 BOTTLE (71335-9679-3)

71335-9679-4 — 60 CAPSULE in 1 BOTTLE (71335-9679-4)

71335-9679-5 — 120 CAPSULE in 1 BOTTLE (71335-9679-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4600 — Zonisamide, 70771-1142 — Zonisamide, 70771-1143 — Zonisamide, 70771-1144 — Zonisamide, 71205-727 — Zonisamide, 71335-0486 — zonisamide, 71335-0962 — Zonisamide, 71335-2796 — Zonisamide, 71335-2797 — Zonisamide, 71335-2798 — Zonisamide, 72189-374 — Zonisamide, 72189-624 — Zonisamide, 72578-040 — Zonisamide, 72578-041 — Zonisamide, 72578-042 — Zonisamide, 76282-226 — Zonisamide, 76282-227 — Zonisamide, 76282-228 — Zonisamide, 80425-0370 — Zonisamide, 80425-0392 — 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.