FDA — authorised 8 May 2003
- Application: ANDA076204
- Marketing authorisation holder: TEVA
- Indication: Labeling
- Status: approved
FDA authorised MOEXIPRIL on 8 May 2003
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 8 May 2003; FDA authorised it on 30 November 2006; FDA authorised it on 30 March 2010.
TEVA holds the US marketing authorisation.