other · Food and Drug Administration · Rule · Published 2006-07-13 · Effective 2006-07-13 · 71 FR 39544
Document
Document number
E6-10973
Federal Register citation
71 FR 39544
CFR reference
21 CFR 522
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2006-07-13
Effective date
2006-07-13
Abstract
The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of four supplemental new animal drug applications (NADAs) filed by Pharmacia & Upjohn Co. The supplemental NADAs establish or revise preslaughter withdrawal periods in cattle injected with a solution made from ceftiofur sodium powder or with a suspension of ceftiofur hydrochloride, or receiving an intramammary infusion of ceftiofur hydrochloride.