NDC 67386-421

Xenazine 12.5 mg tablet

On the label: Lundbeck Pharmaceuticals LLC.

France: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Astrea FontaineFontaine Les Dijon, FranceMakes it Problems found, fixed voluntarilySep 13, 2024 · 4 inspections
Corden Pharma ChenoveChenove, FranceMakes the active ingredient Problems found, fixed voluntarilyFeb 14, 2025 · 5 inspections

Product details

Generic drug
Tetrabenazine: every company that makes it
Form
tablet, oral
Strength
12.5 mg
Approval
NDA NDA021894
On the market since
Nov 24, 2008
Package NDCs
67386-421-01
Official label
DailyMed (National Library of Medicine), updated Nov 1, 2019

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