FDA
- Status: approved
intravenous crystalloid fluid, 500 mL (intravenous crystalloid fluid, 500 mL) 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.
Louisiana State University Health Sciences Center in New Orleans is the originator. The local marketing authorisation holder may differ — check the official source linked above.