federal_register: 2010-2427

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document_number title type abstract publication_date pub_year pub_month html_url pdf_url agency_names agency_ids excerpts
2010-2427 New Animal Drugs for Use in Animal Feeds; Ractopamine; Monensin Rule 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. 2010-02-05 2010 2 https://www.federalregister.gov/documents/2010/02/05/2010-2427/new-animal-drugs-for-use-in-animal-feeds-ractopamine-monensin https://www.govinfo.gov/content/pkg/FR-2010-02-05/pdf/2010-2427.pdf Health and Human Services Department; Food and Drug Administration 221,199 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...

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