NDC 67296-2349

Metaxalone 800 mg tablet

On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-323.

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
Aug 31, 2017
Package NDCs
67296-2349-3
Official label
DailyMed (National Library of Medicine), updated Oct 21, 2026

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