[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2004]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR203.10]

[Page 90]
 
                        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 B_Reimportation
 
Sec. 203.10  Restrictions on reimportation.


    No prescription drug or drug composed wholly or partly of insulin 
that was manufactured in a State and exported from the United States may 
be reimported by anyone other than its manufacturer, except that FDA may 
grant permission to a person other than the manufacturer to reimport a 
prescription drug or insulin-containing drug if it determines that such 
reimportation is required for emergency medical care.