[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2003]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR203.2]

[Page 82-83]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 203--PRESCRIPTION DRUG MARKETING--Table of Contents
 
                      Subpart A--General Provisions
 
Sec. 203.2  Purpose.

    The purpose of this part is to implement the Prescription Drug 
Marketing Act of 1987 and the Prescription Drug

[[Page 83]]

Amendments of 1992, except for those sections relating to State 
licensing of wholesale distributors (see part 205 of this chapter), to 
protect the public health, and to protect the public against drug 
diversion by establishing procedures, requirements, and minimum 
standards for the distribution of prescription drugs and prescription 
drug samples.