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Entreprise · 03/09/20101 min de lecture
Implantation or Injectable Dosage Form New Animal Drugs; Florfenicol and Flunixin
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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 Intervet, Inc. The supplemental NADA adds Mycoplasma bovis to the bovine respiratory disease (BRD) pathogens for which use of an injectable solution containing florfenicol and flunixin meglumine is an approved treatment.
Langue originale de la source: Federal Register — Health and Human ServicesOuvrir le communiqué original →