United States · FDA National Drug Code directory

TEVIMBRA

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
72579-125_d46bfb2e-44c4-4a86-8a8f-b38fb01ac4b6
Product NDC
72579-125
Form
INJECTION, SOLUTION, CONCENTRATE
Composition / generic term
tislelizumab-jsgr
Labeler
BeOne Medicines USA, Inc.
Marketing category
BLA
Marketing start / end (source format)
20260713
Source listing expiry
20271231

Source-listed ingredients

  • TISLELIZUMAB — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, GLASS in 1 CARTON (72579-125-00) / 15 mL in 1 VIAL, GLASS · 72579-125-00

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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TEVIMBRA — United States | Molindra Medicines