FDA
- Status: approved
split-virion, adjuvanted H1N1 vaccine of 7.5 μg per dose (split-virion, adjuvanted H1N1 vaccine of 7.5 μg per dose) regulatory status in United States.
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA has authorised it.
Sinovac Biotech Co., Ltd is the originator. The local marketing authorisation holder may differ — check the official source linked above.