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Entreprise · 11/07/20031 min de lecture
Notice of Approval of New Animal Drug Application; Ivermectin Pour-On
Traduction automatique locale · Langue originale de la source
Résumé
The Food and Drug Administration (FDA) is providing notice that in 2001 it approved a supplemental abbreviated new animal drug application (ANADA) filed by Phoenix Scientific, Inc. The supplemental ANADA provided for topical use of an ivermectin solution on cattle for control of certain internal parasites for 14 days after treatment. The applicable section of the regulation did not require amendment.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →