{"data":{"id":"us/21-cfr-211.196","jurisdiction":"us","citation":"21 CFR 211.196","heading":"Distribution records.","body":"Distribution records shall contain the name and strength of the product and description of the dosage form, name and address of the consignee, date and quantity shipped, and lot or control number of the drug product.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS","Subpart J—Records and Reports"],"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":"fae610d204b48fd2ef90bf0822f94764f5e3636993d60433cba1ac287bc307a4","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-211.194","next":"us/21-cfr-211.198"},"notice":"GroundRules: Original legal text. Not legal advice."}