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Entreprise · 11/05/20091 min de lecture

New Animal Drugs; Trilostane

Traduction automatique locale · Langue originale de la source

Résumé

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect the original approval of a new animal drug application (NADA) filed by Dechra, Ltd. The NADA provides for the veterinary prescription use of trilostane capsules in dogs for treatment of pituitary-dependent hyperadrenocorticism and for treatment of hyperadrenocorticism due to adrenocortical tumor.

Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →

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