FDA — authorised 21 February 1961
- Application: NDA012342
- Marketing authorisation holder: ADVANZ PHARMA
- Status: supplemented
FDA authorised Parnate on 21 February 1961
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 21 February 1961; FDA has authorised it.
ADVANZ PHARMA holds the US marketing authorisation.