New Animal Drugs For Use in Animal Feeds; Ractopamine
other · Food and Drug Administration · Rule · Published 2007-11-23 · Effective 2007-11-23 · 72 FR 65666
Document
Document number
E7-22882
Federal Register citation
72 FR 65666
CFR reference
21 CFR 558
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2007-11-23
Effective date
2007-11-23
Abstract
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Elanco Animal Health. The supplemental NADA provides for an increased level of monensin in two-way combination Type B and Type C medicated feeds containing ractopamine hydrochloride and monensin for cattle fed in confinement for slaughter.