21 CFR § 520.1860 - Pradofloxacin.

---
identifier: "/us/cfr/t21/s520.1860"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 520.1860 - Pradofloxacin."
title_number: 21
title_name: "Food and Drugs"
section_number: "520.1860"
section_name: "Pradofloxacin."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "E"
subchapter_name: "ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS"
part_number: "520"
part_name: "ORAL DOSAGE FORM NEW ANIMAL DRUGS"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 360b."
regulatory_source: "40 FR 13838, Mar. 27, 1975, unless otherwise noted."
cfr_part: "520"
---


# 520.1860 Pradofloxacin.

(a) *Specifications.* Each milliliter of suspension contains 25 milligrams (mg) pradofloxacin.

(b) *Sponsor.* See No. 058198 in § 510.600(c) of this chapter.

(c) *Conditions of use in cats*—(1) *Amount.* Administer 3.4 mg/lb (7.5 mg/kg) body weight once daily for 7 consecutive days.

(2) *Indications for use.* For the treatment of skin infections (wounds and abscesses) in cats caused by susceptible strains of *Pasteurella multocida, Streptococcus canis,* *Staphylococcus aureus, Staphylococcus felis,* and *Staphylococcus pseudintermedius.*

(3) *Limitations.* Federal law prohibits the extralabel use of this drug in food-producing animals. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

[77 FR 76863, Dec. 31, 2012, as amended at 79 FR 28827, May 20, 2014; 86 FR 14819, Mar. 19, 2021]