{"data":{"id":"us/21-cfr-1315.21","jurisdiction":"us","citation":"21 CFR 1315.21","heading":"Individual manufacturing quotas.","body":"The Administrator shall, on or before December 1 of each year, fix for and issue to each person registered to manufacture in bulk ephedrine, pseudoephedrine, or phenylpropanolamine who applies for a manufacturing quota an individual manufacturing quota authorizing that person to manufacture during the next calendar year a quantity of that chemical. Any manufacturing quota fixed and issued by the Administrator is subject to his authority to reduce or limit it at a later date pursuant to § 1315.26 and to his authority to revoke or suspend it at any time pursuant to §§ 1301.36, 1309.43, 1309.44, or 1309.45 of this chapter.","path":["Title 21—Food and Drugs","CHAPTER II—DRUG ENFORCEMENT ADMINISTRATION, DEPARTMENT OF JUSTICE","PART 1315—IMPORTATION AND PRODUCTION QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE","Subpart C—Individual Manufacturing Quotas"],"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":"83f27c6fc4fb675662afb9191302291b0754fe6b17cebc4a5965a7e15922a906","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-1315.13","next":"us/21-cfr-1315.22"},"notice":"GroundRules: Original legal text. Not legal advice."}