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Medicines
Netherlands
Padeliporfin

CBG-MEB 2017

Padeliporfin

Tookad 200 mg poeder voor oplossing voor injectie

Poeder voor oplossing voor injectieNetherlandsAuthorisedAuthorised 10 Nov 2017

Product informationAsk Osler about it

On this page

In other countries
Documents
Sources and licences

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.

TookadEuropean UnionAuthorised

Tookad 183 MG Polvo Para Solucion InyectableSpain · 183 mg · polvo para solución inyectable · Steba Biotech S.A.Same brand
Tookad 366 MG Polvo Para Solucion InyectableSpain · 366 mg · polvo para solución inyectable · Steba Biotech S.A.Same brand
TookadEuropean Union · STEBA Biotech S.ASame brand
TookadCroatiaSame brand
TookadItaly · Polvere per soluzione iniettabile · Steba Biotech S.A.Same brand

Documents

The official texts, at the regulator.

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.

Summary of product characteristicsCBG-MEB

Register entryCBG-MEB

Sources and licences

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

College ter Beoordeling van Geneesmiddelen

College ter Beoordeling van Geneesmiddelen, Geneesmiddeleninformatiebank metadata, source update 07-10-2026; downloaded 08-10-2026; factual adaptation.

Licence: Conditional noncreative administrative factual metadata; no dataset-wide CC0 claim · Added 8 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: Padeliporfin
Dosage form: Poeder voor oplossing voor injectie
Route: Intraveneus gebruik
Register: Netherlands (CBG-MEB)
Status: Authorised
Status in the register: Ingeschreven
Authorised: 10 Nov 2017
Registration: EU/1/17/1228
Marketing authorisation holder: Steba Biotech S.A.
ATC code: L01XD07
Group: Antineoplastic and immunomodulating agents
Procedure: EU centralised
Supply: Uitsluitend recept
EMA product number: EMEA/H/C/004182
EU number: EU/1/17/1228