fbpx

FDA approves higher dose for Rumensin

24-01-2007 | |

The U.S. Food and Drug Administration (FDA) has granted an expanded dose range approval for Rumensin for improvement in feed efficiency and coccidiosis prevention and control in feedlot cattle. The approval increases the upper end of the dose range to 40 grams per ton, on a 90% dry matter basis.

Today, cattle feeders rely on Rumensin – an ionophore used as a feed additive
– from start to finish to prevent and control coccidiosis and to improve feed
efficiency by providing more energy from the ration. By controlling disease and
increasing the efficiency of rumen fermentation, Rumensin reduces feed intake
variation – thus improving rumen function and gastrointestinal
health.

With the approval, the maximum dose increases to 480 mg/hd/d for
feed efficiency for feedlot cattle. For the prevention and control of
coccidiosis, the maximum Rumensin dose also increases to 480 mg/hd/d for feedlot
cattle.

Related link:
Elanco Animal Health

Join 26,000+ subscribers

Subscribe to our newsletter to stay updated about all the need-to-know content in the feed sector, three times a week.
Contributors
Contributors Global Feed Sector Authors
More about