Alert Summary
This WHO Medical Product Alert refers to one batch of falsified OXYCONTIN 80mg (oxycodone hydrochloride). The falsified product was detected in the unregulated market in Switzerland and reported to WHO in February 2025 by the genuine manufacturer MUNDIPHARMA. The falsified product imitates genuine OXYCONTIN 80mg authorized in Poland.
OXYCONTIN (oxycodone hydrochloride) is a semi-synthetic opioid indicated for the treatment of moderate to severe pain.
Laboratory testing of samples of the falsified product was conducted by the Drug Information Centre of the City of Zurich (DIZ), Switzerland. DIZ’s drug checking service determined that the tablets did not contain oxycodone, but a synthetic opioid likely to be a nitazene compound.

