New Animal Drugs for Use in Animal Feeds; Ractopamine
other · Food and Drug Administration · Rule · Published 2008-12-11 · Effective 2008-12-11 · 73 FR 75323
Document
Document number
E8-29177
Federal Register citation
73 FR 75323
CFR reference
21 CFR 558
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2008-12-11
Effective date
2008-12-11
HHS docket
Docket No. FDA-2008-N-0039
Abstract
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (ANADA) filed by Ivy Laboratories, Division of Ivy Animal Health, Inc. The supplemental ANADA provides for an increased level of monensin in four-way combination Type C medicated feeds containing ractopamine, melengestrol, monensin, and tylosin for heifers fed in confinement for slaughter; and a revision to bacterial pathogen nomenclature.