United States · FDA National Drug Code directory

PREVYMIS

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
0006-5085_282d792e-e2f2-4744-8526-4d18427c55cb
Product NDC
0006-5085
Form
PELLET
Composition / generic term
LETERMOVIR
Labeler
Merck Sharp & Dohme LLC
Marketing category
NDA
Marketing start / end (source format)
20240830
Source listing expiry
20271231

Source-listed ingredients

  • LETERMOVIR — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 PACKET in 1 CARTON (0006-5085-01) / 48 PELLET in 1 PACKET · 0006-5085-01

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.

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