NDC 72579-121
Tevimbra 10 mg per 1 mL injection, solution, concentrate
On the label: BeOne Medicines USA, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Boehringer Ingelheim Biopharmaceuticals (China) Ltd. | Shanghai, China | Makes it, makes the active ingredient and tests it | Not inspected on record |
| Novartis Pharma Stein AG | Stein, Switzerland | Makes it and tests it | Problems found, fixed voluntarilyJul 19, 2024 · 9 inspections |
| Novartis d.o.o. | Menges, Slovenia | Makes the active ingredient and tests it | No problems foundSep 21, 2022 · 6 inspections |
| BeOne Pharmaceutical (Suzhou) Co.,Ltd | Suzhou, China | Tests it | Problems found, fixed voluntarilyJun 16, 2023 · 1 inspection |
| Bioreliance Ltd. | Glasgow Lanarkshire, United Kingdom | Tests it | Problems found, fixed voluntarilyMay 13, 2026 · 7 inspections |
| Lek d.d. | Ljubljana, Slovenia | Tests it | Problems found, fixed voluntarilyNov 18, 2025 · 9 inspections |
| Microcoat Biotechnologie GmbH | Bernried, Germany | Tests it | Problems found, fixed voluntarilyJun 27, 2024 · 2 inspections |
| Sharp Packaging Services, LLC | Macungie, PA, United States | Packages it and labels it | Problems found, fixed voluntarilySep 12, 2025 · 6 inspections |
Product details
- Generic drug
- Tislelizumab: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- BLA BLA761232
- On the market since
- Mar 14, 2024
- Package NDCs
72579-121-01- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2026
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