FDA — authorised 2 February 1999
- Application: NDA020886
- Marketing authorisation holder: ADVANZ PHARMA
- Local brand name: PANRETIN
- Indication: GEL — TOPICAL
- Status: approved
FDA authorised Panretin on 2 February 1999
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 2 February 1999; FDA has authorised it.
ADVANZ PHARMA holds the US marketing authorisation.