NDC 68788-7675

Metaxalone 800 mg tablet

On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Lannett Company, Inc.'s NDC 0527-1435.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lannett Company, LLCSeymour, IN, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyOct 21, 2022 · 9 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 ANDA204770
On the market since
Mar 2, 2020
Package NDCs
68788-7675-0 68788-7675-1 68788-7675-2 68788-7675-3 68788-7675-6 68788-7675-9
Official label
DailyMed (National Library of Medicine), updated Jun 17, 2026

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