Oczyesa
The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.
| Name | Oczyesa |
|---|---|
| Active Substance | oktreotidklorid |
| ATC Code | H01CB02 |
| Link to the European Medicines Agency's (EMA) product information | download |
| Link to the European Commission's (EC) decisions | download |
