FDA — authorised 17 September 1976
- Marketing authorisation holder: MOLNLYCKE HLTH
- Status: approved
FDA authorised Exidine on 17 September 1976
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 17 September 1976; FDA authorised it on 24 December 1984; FDA authorised it on 17 December 1985.
MOLNLYCKE HLTH holds the US marketing authorisation.