Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 28 June 2018

Indication(s)

ADENURIC 80 mg film-coated tablets
Treatment of chronic hyperuricaemia in conditions where urate deposition has already occurred (including a history, or presence of, tophus and/or gouty arthritis).

ADENURIC is indicated in adults.


ADENURIC 120 mg film-coated tablets
ADENURIC is indicated for the treatment of chronic hyperuricaemia in conditions where urate deposition has already occurred (including a history, or presence of, tophus and/or gouty arthritis).

ADENURIC is indicated for the prevention and treatment of hyperuricaemia in adult patients undergoing chemotherapy for haematologic malignancies at intermediate to high risk of Tumor Lysis Syndrome (TLS).

ADENURIC is indicated in adults.

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More information

Category Value
Agency product number EMEA/H/C/000777
Orphan designation No
Date First Approved 21-04-2008
Type Medicinal product subject to medical prescription
Marketing authorisation holder Menarini International Operations Luxembourg S.A. (MIOL)