FDA — authorised 16 February 2021
- Application: ANDA208675
- Marketing authorisation holder: SAGENT PHARMS INC
- Status: supplemented
FDA authorised Piperacillin-tazobactam on 16 February 2021 · 3,679 US adverse-event reports
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
Yes. FDA authorised it on 16 February 2021.
SAGENT PHARMS INC holds the US marketing authorisation.