FDA — authorised 19 December 2014
- Application: NDA206829
- Marketing authorisation holder: CUBIST PHARMS LLC
- Local brand name: ZERBAXA
- Indication: POWDER — INTRAVENOUS
- Status: approved
FDA authorised Ceftolozane-tazobactam IV on 19 December 2014
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 19 December 2014.
CUBIST PHARMS LLC holds the US marketing authorisation.