FDA — authorised 1 April 1998
- Application: NDA020816
- Marketing authorisation holder: SANDOZ
- Local brand name: AZOPT
- Indication: SUSPENSION/DROPS — OPHTHALMIC
- Status: approved
FDA authorised Dorzolamide Hcl 2% Oph Soln on 1 April 1998
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 1 April 1998; FDA has authorised it.
SANDOZ holds the US marketing authorisation.