FDA — authorised 17 June 2010
- Application: NDA201023
- Marketing authorisation holder: SANOFI AVENTIS US
- Local brand name: JEVTANA KIT
- Indication: SOLUTION — INTRAVENOUS
- Status: approved
FDA authorised Jevtana Kit on 17 June 2010
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 June 2010.
SANOFI AVENTIS US holds the US marketing authorisation.