FDA — authorised 10 October 1984
- Application: NDA018891
- Marketing authorisation holder: LAVIPHARM
- Status: supplemented
FDA authorised Catapres-TTS-1 on 10 October 1984
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 10 October 1984; FDA has authorised it.
LAVIPHARM holds the US marketing authorisation.