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A first-ever drug for reduction of ammonia gas in livestock has been approved by the U.S. Food and Drug Administration (FDA) for use after being developed by Elanco.

The U.S. Food and Drug Administration has requested that animal drug companies voluntarily revise the labels of drugs intended to treat certain internal parasites in livestock and horses.

New rules shift oversight of ‘medically important’ feed antibiotics from producers to veterinarians.

Bovine spongiform encephalopathy (BSE) has been found on a U.K. farm for the first time since 2015, raising concern that some countries may move to limit imports of British beef.

FDA Commissioner Scott Gottlieb, M.D., issued the following statement on efforts to advance antimicrobial stewardship in veterinary settings.

Testing is underway to determine if four more cows might be infected with bovine spongiform encephalopathy (BSE) on a Scottish farm.

A case of “classical” Bovine Spongiform Encephalopathy (BSE) has left a Scottish farmer devastated and could change the BSE risk status for Scotland, potentially impacting trade.

Officials in Texas have come to a temporary resolution that will allow the use of Cattle Fever Tick spray boxes for 45 days until a permanent solution is found.