Brief: FDA Issues Emergency Use Authorization For Dectomax/Dectomax-Ca1 Injectable Solution
May 19 (Reuters) - FDA: FDA ISSUES EMERGENCY USE AUTHORIZATION FOR OVER-THE-COUNTER INJECTABLE DRUG FOR NEW WORLD SCREWWORM IN DAIRY CATTLE, HORSES, SWINE, SHEEP, DEER FDA: ISSUED EMERGENCY USE AUTHORIZATION FOR DECTOMAX/DECTOMAX-CA1 (DORAMECTIN INJECTION) INJECTABLE SOLUTION Further company coverage: ZTS.N ((Reuters.Briefs@thomsonreuters.com;))
Recent news on Zoetis
See all newsBrief: Zoetis Receives FDA Approval For Convenia® Rtu For Dogs (Cefovecin Injectable Suspension), Helping More Medium And Large Dogs Access Single-Injection Treatment
Brief: FDA Approves Ready-To-Use Cefovecin Injectable For Treatment Of Certain Skin Infections In Dogs
U.S. RESEARCH ROUNDUP-Masco, Sherwin-Williams, Vulcan Materials
Zoetis gets US FDA emergency use nod for treatment for screwworm in dogs
Brief: FDA Issues Emergency Use Authorization For Simparica Trio To Treat New World Screwworm In Dogs, Puppies