Durvalumab
ATC L01FF03 · 11 markets · 25 records
ES 6 records · 1 strengths
- 50 mg/1 mLinjectionIMFINZI
AU 5 records · 5 strengths
- 500 mg/10 mLinjectionIMFINZI
- 120 mg/2.4 mLinjectionIMFINZI
- 500 mginjectionIMFINZI durvalumab (rch) 120 mg concentrated injection vial
- 120 mginjectionIMFINZI durvalumab (rch) 120 mg concentrated injection vial
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
US 4 records · 2 strengths
GB 2 records · 2 strengths
- 500 mg/10 mLinjectionImfinzi 500mg/10ml concentrate for solution for infusion vials
- 120 mg/2.4 mLinjectionImfinzi 500mg/10ml concentrate for solution for infusion vials
HK 2 records · 1 strengths
2 records · 0 manufacturers 2 registros · 0 fabricantes 2 个记录 · 0 个厂家 2 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
CA 1 records · 1 strengths
- 50 mgliquidIMFINZI
SG 1 records · 1 strengths
- 50 mg/mLinjectionIMFINZI CONCENTRATE FOR SOLUTION FOR INFUSION 50 MG/ML
TW 1 records · 1 strengths
- 50 mginjectionIMFINZI Injection 50 mg/ml抑癌寧注射劑
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.
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
FR 1 records · 1 strengths
- 50 mg/1 mLinjectionIMFINZI 50 mg/ml, solution à diluer pour perfusion
| Strength / form / release | US | GB | CA | AU | SG | ES | TW | HK | EU | FR |
|---|---|---|---|---|---|---|---|---|---|---|
| 500 mg/10 mL injection | Manufacturer: Catalent Indiana, LLC ×2 IMFINZI | Imfinzi 500mg/10ml concentrate for solution for infusion vials | IMFINZI | |||||||
| 120 mg/2.4 mL injection | Manufacturer: Catalent Indiana, LLC ×2 IMFINZI | Imfinzi 500mg/10ml concentrate for solution for infusion vials | IMFINZI | |||||||
| 50 mg/1 mL injection | IMFINZI | IMFINZI 50 mg/ml, solution à diluer pour perfusion | ||||||||
| 50 mg injection | IMFINZI Injection 50 mg/ml 抑癌寧注射劑 | |||||||||
| 50 mg liquid | IMFINZI | |||||||||
| 500 mg injection | IMFINZI durvalumab (rch) 120 mg concentrated injection vial | |||||||||
| 120 mg injection | IMFINZI durvalumab (rch) 120 mg concentrated injection vial | |||||||||
| 50 mg/mL injection | IMFINZI CONCENTRATE FOR SOLUTION FOR INFUSION 50 MG/ML | |||||||||
unknown | IMFINZI | IMFINZI CONCENTRATE FOR SOLUTION FOR INFUSION 120MG/2.4ML | IMFINZI |
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Each country column shows the locally registered trade names — not translations.
4 more strength/form rows are recorded only in CA · SG · ES · TW · FR and are not shown in this table. Hay 4 filas de concentración/forma registradas solo en CA · SG · ES · TW · FR que no se muestran en esta tabla. 另有 4 个规格/剂型仅在 CA · SG · ES · TW · FR 有记录(未在本表显示)。 另有 4 個規格/劑型僅在 CA · SG · ES · TW · FR 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.