United States · FDA National Drug Code directory

KEYTRUDA QLEX

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
0006-3083_18b3adae-863b-413b-8e36-e3551115db37
Product NDC
0006-3083
Form
INJECTION, SOLUTION
Composition / generic term
pembrolizumab and berahyaluronidase alfa-pmph
Labeler
Merck Sharp & Dohme LLC
Marketing category
BLA
Marketing start / end (source format)
20250919
Source listing expiry
20271231

Source-listed ingredients

  • PEMBROLIZUMAB — 165 mg/mL
  • BERAHYALURONIDASE ALFA — 2000 U/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (0006-3083-01) / 2.4 mL in 1 VIAL (0006-3083-99) · 0006-3083-01

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.

Browse United States records →