NDC 67386-421 – Xenazine

Tetrabenazine 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67386-421

Product details

Brand name
Xenazine
Generic name
Tetrabenazine
Labeler
Lundbeck Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA021894
Marketed since
November 24, 2008
Listing expires
December 31, 2026
Pharmacologic class
Vesicular Monoamine Transporter 2 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Xenazine →

Package NDC codes (1)

Package NDCDescriptionSince
67386-421-01112 TABLET in 1 BOTTLE (67386-421-01)Nov 24, 2008

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