Business · 19/08/1998Updated: 10/17/2026 · 1 min read

FDA Approves Supplemental New Animal Drug Application for Oxytetracycline Hydrochloride Soluble Powder

Summary

The US Food and Drug Administration (FDA) has amended its animal drug regulations to reflect approval of a supplemental new animal drug application (NADA) filed by Pfizer Inc., allowing for expanded use of oxytetracycline hydrochloride (OTC HCI) soluble powder in various animal species for disease control and treatment.

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

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