NDC 61919-832
Metaxalone 800 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Lannett Company, Inc.'s NDC 0527-1435.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lannett Company, LLC | Seymour, IN, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it and relabels it
Product details
- Generic drug
- Metaxalone: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA204770
- On the market since
- Jun 26, 2019
- Package NDCs
61919-832-30- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
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