FDA — authorised 12 March 1958
- Application: NDA011338
- Marketing authorisation holder: WYETH AYERST
- Local brand name: FLUOTHANE
- Indication: LIQUID — INHALATION
- Status: approved
FDA authorised Anestan on 12 March 1958
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 12 March 1958; FDA authorised it on 9 May 1972; FDA has authorised it.
WYETH AYERST holds the US marketing authorisation.