FDA — authorised 2 August 2006
- Application: NDA021881
- Marketing authorisation holder: SALIX PHARMS
- Local brand name: MOVIPREP
- Indication: FOR SOLUTION — ORAL
- Status: approved
FDA authorised Polyethyleneglycol on 2 August 2006
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 August 2006; FDA has authorised it.
SALIX PHARMS holds the US marketing authorisation.