Avelumab
ATC L01FF04 · 10 markets · 14 records
AU 3 records · 3 strengths
- 200 mg/10 mLinjectionBAVENCIO
- 20 mg/mLinjectionBAVENCIO avelumab (rch) 200 mg/10 mL concentrated solution for intravenous infusion vial
Records without a stated strength · 1 BAVENCIO
ES 3 records · 1 strengths
- 20 mg/1 mLinjectionBAVENCIO
US 1 records · 1 strengths
- 20 mginjectionBAVENCIO
GB 1 records · 1 strengths
- 200 mg/10 mLinjectionBavencio 200mg/10ml concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 20 mgliquidBAVENCIO
SG 1 records · 1 strengths
- 200 mg/10 mLinjectionBAVENCIO CONCENTRATE FOR SOLUTION FOR INFUSION 200MG/10ML
TW 1 records · 1 strengths
- 20 mginjectionBavencio 20mg/mL Concentrate for Solution for Infusion百穩益注射劑20毫克/毫升
HK 1 records · 1 strengths
Records without a stated strength · 1 BAVENCIO CONCENTRATE FOR SOLUTION FOR INFUSION 200MG/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 BAVENCIO
| Strength / form / release | US | GB | CA | AU | SG | ES | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|
| 200 mg/10 mL injection | Bavencio 200mg/10ml concentrate for solution for infusion vials | BAVENCIO | BAVENCIO CONCENTRATE FOR SOLUTION FOR INFUSION 200MG/10ML | ||||||
| 20 mg injection | BAVENCIO | Bavencio 20mg/mL Concentrate for Solution for Infusion 百穩益注射劑20毫克/毫升 | |||||||
| 20 mg liquid | BAVENCIO | ||||||||
| 20 mg/1 mL injection | BAVENCIO | ||||||||
| 20 mg/mL injection | BAVENCIO avelumab (rch) 200 mg/10 mL concentrated solution for intravenous infusion vial | ||||||||
unknown | BAVENCIO | BAVENCIO CONCENTRATE FOR SOLUTION FOR INFUSION 200MG/10ML | BAVENCIO |
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Each country column shows the locally registered trade names — not translations.
2 more strength/form rows are recorded only in CA · ES and are not shown in this table. Hay 2 filas de concentración/forma registradas solo en CA · ES que no se muestran en esta tabla. 另有 2 个规格/剂型仅在 CA · ES 有记录(未在本表显示)。 另有 2 個規格/劑型僅在 CA · ES 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.