NDC 80425-0122

Metaxalone 800 mg tablet

On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Lannett Company, Inc.'s NDC 0527-1435.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lannett Company, LLCSeymour, IN, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyOct 21, 2022 · 9 inspections, 1 with FDA action

Repackaging site

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
80425-0122-1 80425-0122-2 80425-0122-3
Official label
DailyMed (National Library of Medicine), updated Dec 31, 2024

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