NDC 51655-171

Metaxalone 800 mg tablet

On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-650.

United States: 1

Where the pills inside were 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

Repackaging site

Product details

Generic drug
Metaxalone: every company that makes it
Form
tablet, oral
Strength
800 mg
Approval
ANDA ANDA207466
On the market since
Jul 21, 2022
Package NDCs
51655-171-20 51655-171-52
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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