NDC 71335-9679 – Zonisamide

Zonisamide 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-9679

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA214492
Marketed since
July 9, 2021
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
71335-9679-1100 CAPSULE in 1 BOTTLE (71335-9679-1)Apr 6, 2023
71335-9679-290 CAPSULE in 1 BOTTLE (71335-9679-2)Apr 6, 2023
71335-9679-330 CAPSULE in 1 BOTTLE (71335-9679-3)Apr 6, 2023
71335-9679-460 CAPSULE in 1 BOTTLE (71335-9679-4)Apr 6, 2023
71335-9679-5120 CAPSULE in 1 BOTTLE (71335-9679-5)Apr 6, 2023

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