{"data":{"id":"us/21-cfr-520.1880","jurisdiction":"us","citation":"21 CFR 520.1880","heading":"Prednisolone.","body":"(a) Specifications. Each tablet contains 5 or 20 milligrams prednisolone.\n(b) Sponsor. See No. 061690 in § 510.600(c)(2) of this chapter.\n(c) Conditions of use in dogs—(1) Amount. Administer 2.5 milligrams per 4.5 kilograms (10 pounds) body weight per day. Administer total daily dose orally in equally divided doses 6 to 10 hours apart until response is noted or 7 days have elapsed. When response is attained, dosage should be gradually reduced until maintenance level is achieved.\n(2) Indications for use. For use as an anti-inflammatory agent.\n(3) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS","PART 520—ORAL DOSAGE FORM NEW ANIMAL DRUGS"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"e935971d1c46cbcac51a5eb70d65e2a90b2a3813f67c791d4739decf68c1f5db","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-520.1872","next":"us/21-cfr-520.1892"},"notice":"GroundRules: Original legal text. Not legal advice."}