Part 99 — Dissemination of Information on Unapproved/New Uses for Marketed Drugs, Biologics, and Devices
Subpart A — General Information
Subpart B — Information To Be Disseminated
Subpart C — Manufacturer's Submissions, Requests, and Applications
Subpart D — FDA Action on Submissions, Requests, and Applications
Subpart E — Corrective Actions and Cessation of Dissemination
Subpart F — Recordkeeping and Reports