United States · FDA National Drug Code directory
BELSOMRA
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
- 0006-0335_21306af5-e07a-4f8e-8f59-3e0aacc53102
- Product NDC
- 0006-0335
- Form
- TABLET, FILM COATED
- Composition / generic term
- suvorexant
- Labeler
- Merck Sharp & Dohme LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20140829
- Source listing expiry
- 20261231
Source-listed ingredients
- SUVOREXANT — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CASE (0006-0335-13) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 0006-0335-13
- 3 CASE in 1 CARTON (0006-0335-30) / 1 BLISTER PACK in 1 CASE (0006-0335-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 0006-0335-30
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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