NDC 63187-583

Zonisamide 100 mg capsule

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-130.

United States: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Glenmark Pharmaceuticals Inc., USAMonroe, NC, United StatesMakes it and tests it Problems found, fixed voluntarilyJun 17, 2025 · 2 inspections, 1 with FDA action
Glenmark Pharmaceuticals LimitedGoa, IndiaMakes it and tests it Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Zonisamide: every company that makes it
Form
capsule, oral
Strength
100 mg
Approval
ANDA ANDA077651
On the market since
Jan 30, 2006
Package NDCs
63187-583-30 63187-583-60 63187-583-90
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2022

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