NDC 69306-311
Metaxalone 800 mg tablet
On the label: Doc Rx. It's repackaged: Doc 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 |
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
69306-311-2069306-311-3069306-311-6069306-311-90- Official label
- DailyMed (National Library of Medicine), updated Mar 24, 2022
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