{"data":{"id":"us/21-cfr-522.1484","jurisdiction":"us","citation":"21 CFR 522.1484","heading":"Neomycin.","body":"(a) Specifications. Each milliliter of solution contains 50 milligrams (mg) of neomycin sulfate (equivalent to 35 mg of neomycin base).\n(b) Sponsor. See No. 054771 in § 510.600(c) of this chapter.\n(c) Conditions of use in dogs and cats—(1) Amount. Administer 5 mg per pound of body weight daily by intramuscular or intravenous injection, divided into portions administered every 6 to 8 hours for 3 to 5 days.\n(2) Indications for use. For the treatment of acute and chronic bacterial infections due to organisms susceptible to neomycin.\n(3) Limitations. Not for parenteral use in food-producing animals because of prolonged residues in edible tissues. 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 522—IMPLANTATION OR INJECTABLE 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":"2f34c01769422f71717e8831beb6cd639100b017aea93e2cb4f80bd30da6af46","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-522.1468","next":"us/21-cfr-522.1503"},"notice":"GroundRules: Original legal text. Not legal advice."}