Pharmaceutical Business review

Barr receives tentative approval for generic dementia drug

The FDA cannot give final approval until a dispute with Janssen, the new drug application (NDA) holder, Synaptech, the patent owner, and Barr is resolved. In June 2005, Janssen and Synaptech filed suit against Barr Laboratories in the District Court of Delaware to formally initiate the patent challenge process. Trial is set for May 21, 2007.

Razadyne is indicated for the treatment of mild to moderate dementia of the Alzheimer’s type. The product had annual sales of approximately $140 million for the twelve months ending March 2007, according to IMS sales data.