NDC 62756-259 – Zonisamide

Zonisamide 50 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC62756-259

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077634
Marketed since
March 17, 2006
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisamide →

Package NDC codes (4)

Package NDCDescriptionSince
62756-259-0130 CAPSULE in 1 BOTTLE (62756-259-01)Mar 17, 2006
62756-259-02100 CAPSULE in 1 BOTTLE (62756-259-02)Mar 17, 2006
62756-259-03100 CAPSULE in 1 BOTTLE (62756-259-03)Mar 17, 2006
62756-259-041000 CAPSULE in 1 BOTTLE (62756-259-04)Mar 17, 2006

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