NDC 71335-0486 – Zonisamide

Zonisamide 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0486

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077869
Marketed since
July 13, 2016
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisamide →

Package NDC codes (5)

Package NDCDescriptionSince
71335-0486-1100 CAPSULE in 1 BOTTLE (71335-0486-1)Dec 27, 2021
71335-0486-290 CAPSULE in 1 BOTTLE (71335-0486-2)Dec 27, 2021
71335-0486-330 CAPSULE in 1 BOTTLE (71335-0486-3)Dec 27, 2021
71335-0486-460 CAPSULE in 1 BOTTLE (71335-0486-4)Dec 27, 2021
71335-0486-5120 CAPSULE in 1 BOTTLE (71335-0486-5)Dec 27, 2021

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