NDC 52652-8001 – Zonisade

Zonisamide 100 mg/5mL · Suspension · Oral

Human Prescription Drug

Product NDC52652-8001

Product details

Brand name
Zonisade
Generic name
Zonisamide
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Suspension
Route
Oral
Marketing category
NDA · NDA214273
Marketed since
July 15, 2022
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisade →

Package NDC codes (1)

Package NDCDescriptionSince
52652-8001-11 BOTTLE in 1 CARTON (52652-8001-1) / 150 mL in 1 BOTTLEJul 15, 2022