# KIMMTRAK

NDC: 80446-401
Generic name: TEBENTAFUSP
Labeler / Manufacturer: Immunocore Commercial LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20220126

FDA application: BLA761228

## Active ingredients

- TEBENTAFUSP: 100 ug/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80446-401"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80446-401
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24a49f57-d2fc-4ffe-9eb1-fe0460c6b067