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fda press·Jul 15·1 min read
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FDA Grants Emergency Use Authorization for Ivermectin Liquid to Prevent New World Screwworm in Horses

Jul 15, 2026·read at fda press ↗RegulatoryNeutral

The U.S. Food and Drug Administration has issued an Emergency Use Authorization for an ivermectin oral solution intended for horses, aimed at preventing infestations by New World screwworm.

The authorization specifies that the product may be administered within the first 24 hours after birth or at the time a wound is first treated, and it is limited to equine use only.

The decision is presented as part of the current administration’s strategy to shield American agriculture from the threat posed by the parasite, with officials from Health and Human Services and the Department of Agriculture emphasizing its importance.

Authorities said the EUA broadens the nation’s defensive tools and helps protect livestock, wildlife and the surrounding communities.

source

This writeup was produced by pharmadog from original reporting by fda press.

Original headline: “FDA Issues Emergency Use Authorization for Drug for Short-Term Prevention of New World Screwworm in Horses”

read at fda press ↗
801 words · retrieved Jul 29
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IVERMECTIN17MDC-STM17
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Small Molecule5Vaccines

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