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Entreprise · 12/01/20091 min de lecture
Oral Dosage Form New Animal Drugs; Phenylbutazone Tablets and Boluses
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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 First Priority, Inc. The supplemental application provides for revising the description of a 1-gram oral dosage form of phenylbutazone from tablet to bolus.
Langue originale de la source: Federal Register — Food and Drug AdministrationOuvrir le communiqué original →