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Business · 08/06/2006

FDA Approves Oral Dosage Form for Oxibendazole Suspension in Horses

The US Food and Drug Administration (FDA) has amended animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Pfizer, Inc. for revised food safety labeling of oxibendazole suspension administered orally to horses as an antiparasitic treatment.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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