FDA — authorised 21 November 2020
- Marketing authorisation holder: Regeneron Pharmaceuticals, Inc.
- Status: approved
FDA authorised IMDEVIMAB on 21 November 2020
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 November 2020.
Regeneron Pharmaceuticals, Inc. holds the US marketing authorisation.