NDC 69097-861 – Zonisamide

Zonisamide 100 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC69097-861

Product details

Brand name
Zonisamide
Generic name
Zonisamide
Labeler
Cipla USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077869
Marketed since
July 13, 2016
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Zonisamide →

Package NDC codes (2)

Package NDCDescriptionSince
69097-861-07100 CAPSULE in 1 BOTTLE (69097-861-07)Jul 13, 2016
69097-861-12500 CAPSULE in 1 BOTTLE (69097-861-12)Jul 13, 2016

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