Oral Dosage Form New Animal Drugs; Oxytetracycline Hydrochloride Soluble Powder
other · Food and Drug Administration · Rule · Published 2001-05-29 · Effective 2001-05-29 · 66 FR 29019
Document
Document number
01-13379
Federal Register citation
66 FR 29019
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2001-05-29
Effective date
2001-05-29
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 NADA provides for a revised withdrawal time for use of oxytetracycline hydrochloride soluble powder in drinking water of swine.