Department Of Health And Human Services
New Animal Drugs for Use in Animal Feeds; Ractopamine; Monensin
February 5, 2010 - 75 FR 5887 - RIN: - Download Full Notice: Text | PDF
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an original new animal drug application (NADA) filed by Elanco Animal Health, A Division of Eli Lilly & Co. The NADA provides for use of single-ingredient Type A medicated articles containing ractopamine hydrochloride and monensin to formulate two-way combination Type C medicated feeds for finishing hen and tom turkeys.
Agency Contact: Linda M. Wilmot, Center for Veterinary Medicine (HFV-120), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 240-276-8101, e-mail: linda.wilmot@fda.hhs.gov.
This rule is final. Its effective date is February 5, 2010.
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