Oral Dosage Form New Animal Drugs; Oxytetracycline Powder
other · Food and Drug Administration · Rule · Published 2006-12-08 · Effective 2006-12-08 · 71 FR 71038
Document
Document number
E6-20928
Federal Register citation
71 FR 71038
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2006-12-08
Effective date
2006-12-08
Abstract
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a supplemental abbreviated new animal drug application (ANADA) filed by IVX Animal Health, Inc. The supplemental ANADA revises labeling of generic oxytetracycline soluble powder with the current scientific names of the causative bacteria of foulbrood of honeybees.