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EMA Product

Xaluprine (previously Mercaptopurine Nova Laboratories)

Product approved by European Medicines Agency (EU)

Basic Information

Xaluprine (previously Mercaptopurine Nova Laboratories)

Regulatory Information

EMEA/H/C/002022

Authorised

March 9, 2012

July 21, 2011

17

February 13, 2025

Company Information

Ireland

3rd Floor, Ulysses House Foley Street Dublin 1, D01 W2T2

NOVA LABORATORIES IRELAND LIMITED

Active Substances Detail

6-mercaptopurine monohydrate

Detailed Information

Therapeutic Indication

### Therapeutic indication Xaluprine is indicated for the treatment of acute lymphoblastic leukaemia (ALL) in adults, adolescents and children.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Xaluprine. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Xaluprine.

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