{"data":{"id":"us/21-cfr-516.151","jurisdiction":"us","citation":"21 CFR 516.151","heading":"Granting a request for addition to the index.","body":"(a) FDA will grant the request for addition of a new animal drug to the index if none of the reasons described in § 516.149 for denying such a request applies.\n(b) When a request for addition of a new animal drug to the index is granted, FDA will notify the requestor in accordance with § 516.153.","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 516—NEW ANIMAL DRUGS FOR MINOR USE AND MINOR SPECIES","Subpart C—Index of Legally Marketed Unapproved New Animal Drugs for Minor Species"],"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":"9e2c5728379cd10d615b34660cee0910359becd30c1625e54bbf5609374ed350","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-516.149","next":"us/21-cfr-516.153"},"notice":"GroundRules: Original legal text. Not legal advice."}
