StacksVerified U.S. regulatory reference

21 CFR §205.2

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
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.