NDC 45865-355

Baclofen 20 mg tablet

On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Lannett Company, Inc.'s NDC 0527-1337.

United States: 1

Where the pills inside were made

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

Repackaging site

Product details

Generic drug
Baclofen: every company that makes it
Form
tablet
Strength
20 mg
Approval
ANDA ANDA077241
On the market since
Dec 1, 2005
Package NDCs
45865-355-51
Official label
DailyMed (National Library of Medicine), updated Dec 29, 2019

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