Esketamine (marketed as SPRAVATO) has an established regulatory approval and controlled-distribution framework in the European Union for treatment-resistant depression (EMA authorisation), including explicit safety controls requiring supervised administration and monitoring. The European Medicines Agency product assessment and prescribing/safety restrictions are described in the EMA EPAR for SPRAVATO. #
However, Andorra is not an EU Member State and there is no public documentation that SPRAVATO (esketamine nasal spray) is included in a reimbursed national formulary or routinely funded by any Andorran public health reimbursement programme. I found no official Andorran ministry-of-health published reimbursement listing or national guidance making esketamine a reimbursed item; given the country’s small health system and the national drug-control provisions, routine public reimbursement appears not to be in place. Importation or private provision might be possible on a case-by-case basis under hospital procurement or private clinic arrangements, but such access would be exceptional and not a nationally reimbursed pathway. # #