NDC 70332-330
Metaxalone 800 mg tablet
On the label: Fusion Pharmaceuticals LLC. It's repackaged: Fusion Pharmaceuticals LLC 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
- California Pharmaceuticals LLC, Camarillo, California, United States · repackages it
Product details
- Generic drug
- Metaxalone: every company that makes it
- Form
- tablet
- Strength
- 800 mg
- Approval
- ANDA ANDA204770
- On the market since
- Aug 4, 2017
- Package NDCs
70332-330-0170332-330-0270332-330-0370332-330-04- Official label
- DailyMed (National Library of Medicine), updated Jan 2, 2018
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