NDC 50228-192

Lacosamide 50 mg tablet, film coated

On the label: ScieGen Pharmaceuticals, Inc..

United States: 1

Where it's made

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

Product details

Generic drug
Lacosamide: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA205237
On the market since
Mar 18, 2022
Package NDCs
50228-192-10 50228-192-30 50228-192-60
Official label
DailyMed (National Library of Medicine), updated Jun 25, 2026

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