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Oral Dosage Form New Animal Drugs; Toceranib

other · Food and Drug Administration · Rule · Published 2009-06-18 · Effective 2009-06-18 · 74 FR 28874

Document

Document number
E9-14299
Federal Register citation
74 FR 28874
CFR reference
21 CFR 520
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2009-06-18
Effective date
2009-06-18
HHS docket
Docket No. FDA-2009-N-0665

Abstract

The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect the original approval of a new animal drug application (NADA) filed by Pharmacia & Upjohn Co., a Division of Pfizer, Inc. The NADA provides for the veterinary prescription use of toceranib phosphate tablets in dogs for treatment of recurrent, cutaneous mast cell tumors.

Source

Authoritative
Federal Register document
Machine
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