NDC 68682-422 – Tetrabenazine

Tetrabenazine 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68682-422

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
January 31, 2028
Pharmacologic class
Vesicular Monoamine Transporter 2 Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Tetrabenazine →

Package NDC codes (1)

Package NDCDescriptionSince
68682-422-25112 TABLET in 1 BOTTLE (68682-422-25)Jul 20, 2015

Other Tetrabenazine products