{"data":{"id":"us/21-cfr-99.105","jurisdiction":"us","citation":"21 CFR 99.105","heading":"Recipients of information.","body":"A manufacturer disseminating information on a new use under this part may only disseminate that information to a health care practitioner, a pharmacy benefit manager, a health insurance issuer, a group health plan, or a Federal or State Government agency.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER A—GENERAL","PART 99—DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES","Subpart B—Information To Be Disseminated"],"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":"6681c8cffc49734707963a9231e22dd74dcde179b1b902daeccda86b771c3774","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-99.103","next":"us/21-cfr-99.201"},"notice":"GroundRules: Original legal text. Not legal advice."}