NDC 76420-232
Metaxalone 800 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, 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 |
Repackaging site
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it
Product details
- Generic drug
- Metaxalone: every company that makes it
- Form
- tablet, oral
- Strength
- 800 mg
- Approval
- ANDA ANDA204770
- On the market since
- Nov 22, 2016
- Package NDCs
76420-232-2076420-232-3076420-232-6076420-232-90- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2022
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