NDC 69367-332

Levetiracetam ER 500 mg tablet, film coated, extended release

On the label: Westminster Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ScieGen Pharmaceuticals, INC.Hauppauge, NY, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Levetiracetam: every company that makes it
Form
tablet, film coated, extended release, oral
Strength
500 mg
Approval
ANDA ANDA205130
On the market since
Sep 30, 2021
Package NDCs
69367-332-60
Official label
DailyMed (National Library of Medicine), updated Jun 10, 2024

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