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Oral Dosage Form New Animal Drugs; Orbifloxacin

other · Food and Drug Administration · Rule · Published 2006-03-23 · Effective 2006-03-23 · 71 FR 14642

Document

Document number
06-2791
Federal Register citation
71 FR 14642
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2006-03-23
Effective date
2006-03-23

Abstract

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 Schering-Plough Animal Health Corp. The supplemental NADA provides for revised animal safety labeling for orbifloxacin tablets used in dogs and cats for the management of diseases associated with susceptible bacteria.

Source

Authoritative
Federal Register document
Machine
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