[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2007]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR203.10]
[Page 103]
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.
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