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Entreprise · 27/01/20121 min de lecture
Implantation or Injectable Dosage Form New Animal Drugs; Danofloxacin
Traduction automatique locale · Langue originale de la source
Résumé
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 Pfizer, Inc. The supplemental NADA provides for an additional dosage regimen for use of danofloxacin mesylate injectable solution for the treatment of bovine respiratory disease in beef cattle.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →