NDC 68788-7438 – Zonisamide

Zonisamide 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-7438

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077634
Marketed since
March 17, 2006
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisamide →

Package NDC codes (4)

Package NDCDescriptionSince
68788-7438-1100 CAPSULE in 1 BOTTLE (68788-7438-1)Dec 26, 2019
68788-7438-330 CAPSULE in 1 BOTTLE (68788-7438-3)Dec 26, 2019
68788-7438-660 CAPSULE in 1 BOTTLE (68788-7438-6)Dec 26, 2019
68788-7438-990 CAPSULE in 1 BOTTLE (68788-7438-9)Dec 26, 2019

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