# New Animal Drugs for Use in Animal Feeds; Ractopamine; Monensin
> **Food and Drug Administration** · Final rule. · Published 2010-02-05 · Effective 2010-02-05 · 75 FR 5887
## Document
- **Document number:** 2010-2427
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 75 FR 5887
- **CFR reference:** 21 CFR 558
- **Publication date:** 2010-02-05
- **Effective date:** 2010-02-05
- **HHS docket:** Docket No. FDA-2010-N-0002
## Abstract

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.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2010/02/05/2010-2427/new-animal-drugs-for-use-in-animal-feeds-ractopamine-monensin)
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