FDA — authorised 2 February 1979
- Application: NDA017378
- Marketing authorisation holder: BAXTER HLTHCARE
- Status: supplemented
🇺🇸 Plasma-lyte in United States
FDA authorised Plasma-lyte on 2 February 1979
Marketing authorisation
Other Critical Care / Fluid and Electrolyte Management approved in United States
Frequently asked questions
Is Plasma-lyte approved in United States?
Yes. FDA authorised it on 2 February 1979.
Who is the marketing authorisation holder for Plasma-lyte in United States?
BAXTER HLTHCARE holds the US marketing authorisation.