ZONISADE
NDC 52652-8001 · Azurity Pharmaceuticals, Inc.
Generic nameZONISAMIDE
Dosage formSUSPENSION
RouteORAL
Active ingredient(s)ZONISAMIDE
Strength100 mg/5mL
Pharmacologic classAnti-epileptic Agent [EPC], Carbonic Anhydrase Inhibitors [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], P-Glycoprotein Inhibitors [MoA], Sulfonamides [CS]
Marketing categoryNDA
Packages
52652-8001-1 — 1 BOTTLE in 1 CARTON (52652-8001-1) / 150 mL in 1 BOTTLE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0615-8266 — zonisamide, 29300-428 — Zonisamide, 29300-429 — Zonisamide, 29300-430 — Zonisamide, 50268-816 — 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, 62756-260 — Zonisamide, 63187-583 — Zonisamide, 63187-897 — Zonisamide, 63629-3293 — Zonisamide, 68001-242 — Zonisamide, 68001-243 — Zonisamide, 68001-244 — Zonisamide, +30 more