FDA — authorised 7 April 1960
- Application: NDA012283
- Marketing authorisation holder: SANOFI AVENTIS US
- Local brand name: HYGROTON
- Indication: TABLET — ORAL
- Status: approved
FDA authorised Chlorthalidone with potassium chloride on 7 April 1960
Yes. FDA authorised it on 7 April 1960.
SANOFI AVENTIS US holds the US marketing authorisation.