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Geschäft · 18.11.19961 Min. Lesezeit
Countrymark Cooperative, Inc.; Withdrawal of Approval of NADA
Lokale automatische Übersetzung · Originalsprache der Quelle
Zusammenfassung
The Food and Drug Administration (FDA) is withdrawing approval of a new animal drug application (NADA) held by Countrymark Cooperative, Inc. The NADA provides for the use of tylosin Type A medicated articles to make Type C medicated feeds. Countrymark Cooperative requested the withdrawal of approval of the NADA because they are no longer making Type A medicated articles for use in Type C medicated feeds. In a final rule published elsewhere in this issue of the Federal Register, FDA is amending the regulations by removing those entries which reflect approval of the NADA.
Originalsprache der Quelle: Federal Register — Food and Drug AdministrationOriginalquelle öffnen →