Dostarlimab
ATC L01FF07 · 10 markets · 13 records
AU 3 records · 3 strengths
- 500 mg/10 mLinjectionJemperli
- 500 mg/mLinjectionJEMPERLI dostarlimab 500 mg concentrate for solution for infusion 10 mL vial
Records without a stated strength · 1 Jemperli
ES 2 records · 1 strengths
- 500 mginjectionJemperli
US 1 records · 1 strengths
- 50 mginjectionJemperli
GB 1 records · 1 strengths
- 500 mg/10 mLinjectionJemperli 500mg/10ml concentrate for solution for infusion vials
CA 1 records · 1 strengths
- 50 mgliquidJemperli
SG 1 records · 1 strengths
- 500 mg/10 mLinjectionJEMPERLI CONCENTRATE FOR SOLUTION FOR INFUSION 500MG/10ML
MX 1 records · 1 strengths
Records without a stated strength · 1 Jemperli
TW 1 records · 1 strengths
- 50 mginjectionJEMPERLI Concentrate for Solution for Infusion 50 mg/mL健沛利濃縮輸注液50毫克/毫升
HK 1 records · 1 strengths
Records without a stated strength · 1 JEMPERLI CONCENTRATE FOR SOLUTION FOR INFUSION 500MG/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 Jemperli
| Strength / form / release | US | GB | CA | AU | SG | ES | MX | TW | HK | EU |
|---|---|---|---|---|---|---|---|---|---|---|
| 500 mg/10 mL injection | Jemperli 500mg/10ml concentrate for solution for infusion vials | Jemperli | JEMPERLI CONCENTRATE FOR SOLUTION FOR INFUSION 500MG/10ML | |||||||
| 50 mg injection | Jemperli | JEMPERLI Concentrate for Solution for Infusion 50 mg/mL 健沛利濃縮輸注液50毫克/毫升 | ||||||||
| 50 mg liquid | Jemperli | |||||||||
| 500 mg injection | Jemperli | |||||||||
| 500 mg/mL injection | JEMPERLI dostarlimab 500 mg concentrate for solution for infusion 10 mL vial | |||||||||
unknown | Jemperli | JEMPERLI CONCENTRATE FOR SOLUTION FOR INFUSION 500MG/10ML | Jemperli | |||||||
liquid | Jemperli |
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Each country column shows the locally registered trade names — not translations.
3 more strength/form rows are recorded only in CA · ES · MX and are not shown in this table. Hay 3 filas de concentración/forma registradas solo en CA · ES · MX que no se muestran en esta tabla. 另有 3 个规格/剂型仅在 CA · ES · MX 有记录(未在本表显示)。 另有 3 個規格/劑型僅在 CA · ES · MX 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.