Durvalumab
ATC L01FF03 · 10 markets · 24 records
Durvalumab
Forms
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
Records without a stated strength · 1 IMFINZI
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
Records without a stated strength · 1 IMFINZI CONCENTRATE FOR SOLUTION FOR INFUSION 120MG/2.4ML
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.
Records without a stated strength · 1 IMFINZI
The same ingredient can carry completely different
brand names in different countries, and the same name can point to a different ingredient.
Listed by country — not interchangeable.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.
A side-by-side table is offered only when this ingredient has records in many markets; otherwise this list is the whole picture.