Dostarlimab

JEMPERLI 500 mg CONCENTRADO PARA SOLUCION PARA PERFUSION

500 mg concentrado para solución para perfusiónSpainMarketedAuthorised 24 May 2021

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In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

JemperliEuropean UnionAuthorised

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

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Dostarlimab

JEMPERLI 500 mg CONCENTRADO PARA SOLUCION PARA PERFUSION

500 mg concentrado para solución para perfusiónSpainMarketedAuthorised 24 May 2021

Product informationAsk Osler about it

In other countries

The same active substances on other registers, the same brand first.

Authorised centrally in the EU

This national listing belongs to a medicine the European Commission authorised for the whole EU.

JemperliEuropean UnionAuthorised

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Discover Osler

Jemperli Concentrate for Solution for Infusion 500MG/10MLSingapore · 500mg/10mL · infusion, solution concentrate · Glaxosmithkline Pte LTD

JemperliUnited States · 500MG/10ML · injectable · Glaxosmithkline

Packs

Pack	Code	Status
JEMPERLI 500 mg CONCENTRADO PARA SOLUCION PARA PERFUSION, 1 vial de 10 ml	730927

Documents

The official texts, at the regulator.

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

Agencia Española de Medicamentos y Productos Sanitarios

Fuente de la información: Agencia Española de Medicamentos y Productos Sanitarios www.aemps.gob.es; CIMA medicamentos, acquired 11 October 2026 UTC; each source response/update date retained.

Licence: AEMPS explicit public open-data reuse for citizens and companies; source attribution and update date required · Added 12 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Dostarlimab
Strength: 500 mg
Dosage form: concentrado para solución para perfusión
Route: vía intravenosa
Register: Spain (AEMPS)
Status: Marketed
Status in the register: Autorizado, comercializado
Authorised: 24 May 2021
Registration: 1211538001
Marketing authorisation holder: Glaxosmithkline Trading Services Limited
Procedure: EU centralised
Supply: Uso Hospitalario
EU number: EU/1/21/1538