NDC 68682-421 – Tetrabenazine

Tetrabenazine 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68682-421

Product details

Brand name
Tetrabenazine
Generic name
Tetrabenazine
Labeler
Oceanside Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021894
Marketed since
July 20, 2015
Marketing end
December 31, 2026
Pharmacologic class
Vesicular Monoamine Transporter 2 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tetrabenazine →

Package NDC codes (1)

Package NDCDescriptionSince
68682-421-12112 TABLET in 1 BOTTLE (68682-421-12)Jul 20, 2015

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