Esketamine nasal spray (Spravato) received a marketing authorisation valid throughout the EU on 18 December 2019 via the European Commission; the EMA summary and EPAR describe its indication for adults with treatment‑resistant major depressive disorder in combination with an SSRI/SNRI and special supervised administration requirements. Access in Cyprus therefore is technically permitted under EU authorisation, but inclusion in public reimbursement lists (the national formulary under the Health Insurance Organization / GeSY) and practical availability depend on national pricing/reimbursement decisions and provider arrangements. There is no evidence of an automatic, universal public reimbursement for Spravato in Cyprus — access will generally require (a) a prescribing psychiatrist, (b) treatment provision in an authorised supervised setting (per the EU/EMA conditions), and (c) either private payment or case-by-case approval through national reimbursement procedures or specialty funding channels. Citations: EMA authorisation and product information for Spravato. # Additionally, national reimbursement and formulary inclusion in Cyprus is governed by HIO/GeSY processes and a national formulary committee; reimbursement decisions are not automatic following EU authorisation. #