Regulations last checked for updates: Oct 17, 2024

Title 21 - Food and Drugs last revised: Oct 15, 2024
§ 205.2 - Purpose.

The purpose of this part is to implement the Prescription Drug Marketing Act of 1987 by providing minimum standards, terms, and conditions for the licensing by State licensing authorities of persons who engage in wholesale distributions in interstate commerce of prescription drugs.

authority: 21 U.S.C. 351,352,353,371,374
source: 55 FR 38023, Sept. 14, 1990, unless otherwise noted.
cite as: 21 CFR 205.2