Tislelizumab
ATC L01FF09 · 10 markets · 15 records
US 3 records · 1 strengths
- 10 mginjectionTEVIMBRAManufacturer: Novartis Pharma Stein AG
AU 3 records · 3 strengths
- 100 mg/10 mLinjectionTEVIMBRA
- 100 mginjectionTEVIMBRA tislelizumab 100 mg/10 mL concentrated injection vial
Records without a stated strength · 1 TEVIMBRA
GB 1 records · 1 strengths
- 100 mg/10 mLinjectionTevimbra 100mg/10ml concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 10 mg/1 mLliquidTEVIMBRA
SG 1 records · 1 strengths
- 100 mg/10 mLinjectionTEVIMBRA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML
CN 1 records · 1 strengths
- 100 mg/10 mLinjection百泽安替雷利珠单抗
ES 1 records · 1 strengths
- 100 mginjectionTEVIMBRA
TW 1 records · 1 strengths
Records without a stated strength · 1 Tevimbra Concentrated Solution for Infusion、汰瘤安注射劑
HK 1 records · 1 strengths
Records without a stated strength · 1 TEVIMBRA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML
EU 1 records · 1 strengths
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Records without a stated strength · 1 TEVIMBRA
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 100 mg/10 mL injection | Tevimbra 100mg/10ml concentrate for solution for infusion vials | TEVIMBRA | TEVIMBRA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML | 百泽安替雷利珠单抗 | ||||||
| 100 mg injection | TEVIMBRA tislelizumab 100 mg/10 mL concentrated injection vial | TEVIMBRA | ||||||||
| 10 mg injection | Manufacturer: Novartis Pharma Stein AG TEVIMBRA | |||||||||
| 10 mg/1 mL liquid | TEVIMBRA | |||||||||
unknown | TEVIMBRA | TEVIMBRA CONCENTRATE FOR SOLUTION FOR INFUSION 100MG/10ML | TEVIMBRA | |||||||
injection | Tevimbra Concentrated Solution for Infusion 汰瘤安注射劑 |
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Each country column shows the locally registered trade names — not translations.
1 more strength/form rows are recorded only in CA and are not shown in this table. Hay 1 filas de concentración/forma registradas solo en CA que no se muestran en esta tabla. 另有 1 个规格/剂型仅在 CA 有记录(未在本表显示)。 另有 1 個規格/劑型僅在 CA 有記錄(未在本表顯示)。
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.