United States · FDA National Drug Code directory
KIMMTRAK
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
- 80446-401_6da26ba2-92a2-4c0f-b733-946f25c71338
- Product NDC
- 80446-401
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- TEBENTAFUSP
- Labeler
- Immunocore Commercial LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 20220126
- Source listing expiry
- 20271231
Source-listed ingredients
- TEBENTAFUSP — 100 ug/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (80446-401-01) / .5 mL in 1 VIAL, GLASS · 80446-401-01
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 →