21 CFR § 99.105 - Recipients of information.

---
identifier: "/us/cfr/t21/s99.105"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 99.105 - Recipients of information."
title_number: 21
title_name: "Food and Drugs"
section_number: "99.105"
section_name: "Recipients of information."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "A"
subchapter_name: "GENERAL"
part_number: "99"
part_name: "DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 321, 331, 351, 352, 355, 360, 360c, 360e, 360aa-360aaa-6, 371, and 374; 42 U.S.C. 262."
regulatory_source: "63 FR 64581, Nov. 20, 1998, unless otherwise noted."
cfr_part: "99"
---


# 99.105 Recipients of information.

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.