Implantation or Injectable Dosage Form New Animal Drugs; Ceftiofur Crystalline Free Acid
other · Food and Drug Administration · Rule · Published 2008-10-08 · Effective 2008-10-08 · 73 FR 58871
Document
Document number
E8-23830
Federal Register citation
73 FR 58871
CFR reference
21 CFR 522
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2008-10-08
Effective date
2008-10-08
HHS docket
Docket No. FDA-2008-N-0039
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 Pharmacia & Upjohn Co., a Division of Pfizer, Inc. The supplemental NADA provides for veterinarian prescription use of ceftiofur crystalline free acid injectable suspension for the treatment of bovine foot rot (interdigital necrobacillosis).