Visudyne
·
- Prescription status not stated
- Eyes and ears
- Active substance
- Verteporfin
- Used in
- Eyes and ears
- Made by
- CHEPLAPHARM Arzneimittel GmbH
- Source
- Official label
Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.
What it is for
- Visudyne is indicated for the treatment of: adults with exudative (wet) age-related macular degeneration (AMD) with predominantly classic subfoveal choroidal neovascularisation (CNV) or; adults with subfoveal choroidal neovascularisation secondary to pathological myopia.
From the official label · 2026-09-30 · European Medicines Agency
Same active substance, strength and form in other countries
Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.
Medicine passport: one printable page to show a pharmacist abroad
SpainNo exact match for this strength and form
CanadaNo exact match for this strength and form
NetherlandsNo exact match for this strength and form
SwitzerlandNo exact match for this strength and form
Details
| Made by | CHEPLAPHARM Arzneimittel GmbH |
|---|---|
| Active substance | Verteporfin |
| Used in | Eyes and ears |
| Classification | S01LA01 · Eyes and ears |
| Authorised on | 2000-07-27 |
| Last updated by the regulator | 2020-09-16 |
| EMA product number | EMEA/H/C/000305 |
Source: European Medicines Agency — medicine data · 2026-09-30 · not reviewed by a clinician
Source: European Medicines Agency (EMA). Product information as published by EMA. Reuse terms: EMA legal notice (reproduction authorised).