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
0006-0005_21306af5-e07a-4f8e-8f59-3e0aacc53102
Product NDC
0006-0005
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 — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BLISTER PACK in 1 CASE (0006-0005-13) / 3 TABLET, FILM COATED in 1 BLISTER PACK · 0006-0005-13
  • 3 CASE in 1 CARTON (0006-0005-30) / 1 BLISTER PACK in 1 CASE (0006-0005-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 0006-0005-30

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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