{"data":{"id":"us/21-cfr-226.80","jurisdiction":"us","citation":"21 CFR 226.80","heading":"Packaging and labeling.","body":"(a) Packaging and labeling operations shall be adequately controlled:\n(1) To assure that only those Type A medicated article(s) that have met the specifications established in the master-formula records shall be distributed.\n(2) To prevent mixups during the packaging and labeling operations.\n(3) To assure that correct labeling is employed for each Type A medicated article(s).\n(4) To identify Type A medicated article(s) with lot or control numbers that permit determination of the history of the manufacture and control of the batch of Type A medicated article(s).\n(b) Packaging and labeling operations shall provide:\n(1) For storage of labeling in a manner to avoid mixups.\n(2) For careful checking of labeling for identity and conformity to the labeling specified in the batch-production records.\n(3) For adequate control of the quantities of labeling issued for use with the Type A medicated article(s).\n(c) Type A medicated article(s) shall be distributed in suitable containers to insure the safety, identity, strength, and quality of the finished product.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES","Subpart D—Packaging and Labeling"],"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":"44d6ce660d332e2673dd44e770b62619d4e94b8cb5dbe2ca6e01ceec89ddc36e","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-226.58","next":"us/21-cfr-226.102"},"notice":"GroundRules: Original legal text. Not legal advice."}