FDA — authorised 24 July 1992
- Marketing authorisation holder: GLAXOSMITHKLINE
- Status: approved
FDA authorised Halfan on 24 July 1992
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 24 July 1992.
GLAXOSMITHKLINE holds the US marketing authorisation.