Oral Dosage Form New Animal Drugs; Oxytetracycline
other · Food and Drug Administration · Rule · Published 2006-06-27 · Effective 2006-06-27 · 71 FR 36483
Document
Document number
E6-10053
Federal Register citation
71 FR 36483
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2006-06-27
Effective date
2006-06-27
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 Pfizer, Inc. The supplemental NADA revises labeling of oxytetracycline soluble powder with the current genus for the causative bacteria for American foul brood of honeybees.