NDC 70518-0771
Metaxalone 800 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
Product details
- Generic drug
- Metaxalone: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA204770
- On the market since
- Oct 9, 2017
- Package NDCs
70518-0771-070518-0771-170518-0771-270518-0771-370518-0771-4- Official label
- DailyMed (National Library of Medicine), updated Jun 30, 2026
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