INDIANAPOLIS, INDIANA, April 27, 2026
Elanco Animal Health has received Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) and a Section 18 Emergency Exemption from the U.S. Environmental Protection Agency (EPA) for its products Negasunt™ Powder and Tanidil™, aimed at preventing and treating New World screwworm infestations in livestock, marking a critical step in safeguarding animal health against an emerging parasitic threat. These authorizations, issued in coordination with the U.S. Department of Agriculture (USDA), ensure that veterinarians and livestock producers are equipped with immediate, science-based solutions to respond rapidly to potential outbreaks, particularly as confirmed cases have been detected near the U.S.-Mexico border.
Emergency Authorization Strengthens Disease Preparedness
The FDA’s EUA for Negasunt Powder and EPA’s emergency exemption for Tanidil provide essential tools for early intervention against New World screwworm infestations, a serious parasitic condition caused by larvae that invade open wounds in animals. This coordinated regulatory action reflects the urgency of addressing potential outbreaks and highlights the importance of preparedness in protecting livestock populations and agricultural economies.
The products will be distributed through the U.S. Animal and Plant Health Inspection Service (APHIS) and its National Veterinary Stockpile, ensuring controlled access and proper oversight. Their use will be limited to authorized personnel, including veterinarians and trained professionals operating within designated zones, with strict compliance requirements for safety, tracking, and reporting.
These measures underscore the collaborative efforts of federal agencies to mitigate the risk of widespread infestation, reinforcing the role of regulatory frameworks in enabling rapid response to emerging animal health threats.

