この記事の翻訳を準備しています。それまでの間、英語の原文を表示します。
規制と法律 · 1996/11/181 分で読めます
Animal Drugs, Feeds, and Related Products; Tylosin
ローカル自動翻訳 · 情報源の原言語
概要
The Food and Drug Administration (FDA) is amending the animal drug regulations to remove that portion reflecting approval of a new animal drug application (NADA) held by Countrymark Cooperative, Inc. (formerly Indiana Farm Bureau Cooperative Association, Inc.). The NADA provides for use of a tylosin Type A medicated article for making a tylosin Type C medicated swine feed. In a notice published elsewhere in this issue of the Federal Register, FDA is withdrawing approval of the NADA.
情報源の原言語: Federal Register — All Documents原文の発表を開く →