FDA — authorised 15 April 2016
- Application: NDA203324
- Marketing authorisation holder: GLAUKOS
- Status: supplemented
FDA authorised Cross linking on 15 April 2016
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 15 April 2016; FDA authorised it on 17 October 2025; FDA has authorised it.
GLAUKOS holds the US marketing authorisation.