FDA — authorised 20 August 1963
- Application: NDA013157
- Marketing authorisation holder: LILLY
- Local brand name: ANHYDRON
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Ciclotiazide on 20 August 1963
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Yes. FDA authorised it on 20 August 1963; FDA authorised it on 8 June 1982; FDA authorised it on 8 June 1982.
LILLY holds the US marketing authorisation.