[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: 21CFR203.1]
[Page 100]
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. 203.1 Scope.
This part sets forth procedures and requirements pertaining to the
reimportation and wholesale distribution of prescription drugs,
including both bulk drug substances and finished dosage forms; the sale,
purchase, or trade of (or the offer to sell, purchase, or trade)
prescription drugs, including bulk drug substances, that were purchased
by hospitals or health care entities, or donated to charitable
organizations; and the distribution of prescription drug samples. Blood
and blood components intended for transfusion are excluded from the
restrictions in and the requirements of the Prescription Drug Marketing
Act of 1987 and the Prescription Drug Amendments of 1992.
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