{"data":{"id":"us/21-cfr-330.3","jurisdiction":"us","citation":"21 CFR 330.3","heading":"Imprinting of solid oral dosage form drug products.","body":"A requirement to imprint an identification code on solid oral dosage form drug products is set forth under part 206 of this chapter.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER D—DRUGS FOR HUMAN USE","PART 330—OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED","Subpart A—General Provisions"],"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":"11ece194df739cc5caec08607a6a76f9a107480650746702984d5f7381f51147","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-330.2","next":"us/21-cfr-330.5"},"notice":"GroundRules: Original legal text. Not legal advice."}