FDA — authorised 15 December 2015
- Application: NDA022225
- Marketing authorisation holder: MSD SUB MERCK
- Local brand name: BRIDION
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised deep block on 15 December 2015
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 December 2015; FDA has authorised it.
MSD SUB MERCK holds the US marketing authorisation.