FDA — authorised 27 September 1978
- Application: NDA017512
- Marketing authorisation holder: VANTIVE US HLTHCARE
- Status: supplemented
FDA authorised Dianeal on 27 September 1978
Yes. FDA authorised it on 27 September 1978; FDA authorised it on 4 December 1992; FDA authorised it on 4 December 1992.
VANTIVE US HLTHCARE holds the US marketing authorisation.