NDC 68462-128 – Zonisamide

Zonisamide 25 mg/1 · Capsule · Oral

Human Prescription Drug 5 recalls

Product NDC68462-128

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077651
Marketed since
January 30, 2006
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisamide →

Package NDC codes (2)

Package NDCDescriptionSince
68462-128-01100 CAPSULE in 1 BOTTLE (68462-128-01)Jan 30, 2006
68462-128-05500 CAPSULE in 1 BOTTLE (68462-128-05)Jan 30, 2006

Recalls mentioning this NDC

Other Zonisamide products