United States · FDA National Drug Code directory
tetrabenazine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 68682-422_66a8dcef-cfb3-484a-a213-658943881951
- Product NDC
- 68682-422
- Form
- TABLET
- Composition / generic term
- tetrabenazine
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20150720 / 20280131
Source-listed ingredients
- TETRABENAZINE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 112 TABLET in 1 BOTTLE (68682-422-25) · 68682-422-25
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →