FDA Approves Exzolt Cattle-CA1 for Prevention and Treatment of New World Screwworm
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FDA Approves Exzolt Cattle-CA1 for Prevention and Treatment of New World Screwworm

On December 4, 2025, the U.S. Food and Drug Administration (FDA) granted conditional approval to Exzolt Cattle-CA1, a fluralaner topical solution from Merck Animal Health, for the use in beef cattle (≥ 2 months of age) and replacement dairy heifers (< 20 months of age). The approved uses include prevention and treatment of larval infestations by New World screwworm (NWS), and treatment and control of cattle fever tick.

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The Feline Veterinary Medical Association and Merck Animal Health Champion Future Leaders in Feline Medicine
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The Feline Veterinary Medical Association and Merck Animal Health Champion Future Leaders in Feline Medicine

The Feline Veterinary Medical Association (FelineVMA) and Merck Animal Health are delighted to announce the 2025 Scholarships for Academic Excellence in Feline Healthcare recipients. This year’s recipients are Holly Kessler, The Ohio State University, Class of 2027, and Claire Stratton, Colorado State University, Class of 2026. Both recipients receive a $10,000 scholarship and a complimentary registration to the 2025 FelineVMA Annual Conference for their passion for feline medicine and a desire to elevate feline healthcare.

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FDA Approves New Oral Treatment for Poultry Mites
Jill Lopez Jill Lopez

FDA Approves New Oral Treatment for Poultry Mites

A new approach to controlling northern fowl mites, a common parasite in poultry, has received approval from the U.S. Food and Drug Administration (FDA)—and Penn State researchers played a key role in the process.

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Merck Animal Health Receives Positive Opinion from EU CVMP for Numelvi Tablets for Dogs
Jill Lopez Jill Lopez

Merck Animal Health Receives Positive Opinion from EU CVMP for Numelvi Tablets for Dogs

Merck Animal Health, known as MSD Animal Health outside the United States and Canada, a division of Merck & Co., Inc., has announced that the European Medicines Agency’s Committee for Veterinary Medicinal Products (CVMP) has issued a positive opinion for Numelvi (atinvicitinib) tablets for dogs. This marks an important step toward the availability of Numelvi in the European Union.

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