FDA — authorised 22 January 1992
- Application: NDA020098
- Marketing authorisation holder: ABBVIE
- Local brand name: MIVACRON
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised Mivacron on 22 January 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 22 January 1992; FDA has authorised it.
ABBVIE holds the US marketing authorisation.