[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2002]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR226.110]

[Page 150]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 226--CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES--Table of Contents
 
                     Subpart E--Records and Reports
 
Sec. 226.110  Distribution records.

    Complete records shall be maintained for each shipment of Type A 
medicated article(s) in a manner that will facilitate the recall, 
diversion, or destruction of the Type A medicated article(s), if 
necessary. Such records shall be retained for at least 2 years after the 
date of the shipment by the manufacturer and shall include the name and 
address of the consignee, the date and quantity shipped, and the 
manufacturing dates, control numbers, or marks identifying the Type A 
medicated article(s) shipped.