FDA Webview
X

Free FDA Notices

Review Period Set for Alamast

03/23/2006

Federal Register Notice: FDA has determined the regulatory review period for Santen Pharmaceutical Co.’s Alamast (pemirolast potassium) is 1,298 days for extending a patent that claims the human drug product. Alamast is indicated for preventing itching of the eye due to allergic conjunctivitis. To view this notice, click here.

LATEST NEWS