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
- 47335-179_86ebe1dd-8c77-4615-8a4c-1e8ec4dc0098
- Product NDC
- 47335-179
- Form
- TABLET
- Composition / generic term
- Tetrabenazine
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150817
- Source listing expiry
- 20261231
Source-listed ingredients
- TETRABENAZINE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 112 TABLET in 1 BOTTLE (47335-179-23) · 47335-179-23
Source and coverage
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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.
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