Toripalimab
ATC L01FF13 · 9 markets · 13 records
AU 3 records · 3 strengths
- 240 mg/6 mLinjectionZytorvi
- 240 mginjectionZYTORVI toripalimab 240 mg/ 6 mL concentrated injection vial
Records without a stated strength · 1 Zytorvi
CN 3 records · 3 strengths
US 1 records · 1 strengths
- 240 mg/6 mLinjectionLOQTORZI
GB 1 records · 1 strengths
- 240 mg/6 mLinjectionLoqtorzi 240mg/6ml concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 40 mgliquidLOQTORZI
SG 1 records · 1 strengths
- 240 mg/6 mLinjectionLOQTORZI CONCENTRATE FOR SOLUTION FOR INFUSION 240MG/6ML
ES 1 records · 1 strengths
- 240 mginjectionLOQTORZI
HK 1 records · 1 strengths
Records without a stated strength · 1 LOQTORZI CONCENTRATE FOR SOLUTION FOR INFUSION 240MG/6ML
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 LOQTORZI
| Strength / form / release | US | GB | CA | AU | SG | CN | ES | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 240 mg/6 mL injection | LOQTORZI | Loqtorzi 240mg/6ml concentrate for solution for infusion vials | Zytorvi | LOQTORZI CONCENTRATE FOR SOLUTION FOR INFUSION 240MG/6ML | |||||
| 240 mg injection | ZYTORVI toripalimab 240 mg/ 6 mL concentrated injection vial | 拓益特瑞普利单抗 | LOQTORZI | ||||||
| 40 mg liquid | LOQTORZI | ||||||||
| 100 mg injection | 拓益特瑞普利单抗 | ||||||||
| 80 mg injection | 拓益特瑞普利单抗 | ||||||||
unknown | Zytorvi | LOQTORZI CONCENTRATE FOR SOLUTION FOR INFUSION 240MG/6ML | LOQTORZI |
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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.