NDC 68001-485

Metaxalone 800 mg tablet

On the label: BluePoint Laboratories..

United States: 1

Where it's made

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

Product details

Generic drug
Metaxalone: every company that makes it
Form
tablet, oral
Strength
800 mg
Approval
ANDA ANDA207466
On the market since
May 31, 2021
Package NDCs
68001-485-00
Official label
DailyMed (National Library of Medicine), updated Jul 7, 2025

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