[Code of Federal Regulations]
[Title 21, Volume 4]
[Revised as of April 1, 2001]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR225.142]

[Page 143]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                                SERVICES
 
PART 225--CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS--Table of Contents
 
                  Subpart G--Product Quality Assurance
 
Sec. 225.142  Components.

    Source: 51 FR 7390, Mar. 3, 1986, unless otherwise noted.


    Adequate procedures shall be established and maintained for the 
identification, storage, and inventory control (receipt and use) of all 
Type A medicated articles and Type B medicated feeds intended for use in 
the manufacture of medicated feeds to aid in assuring the identity, 
strength, quality, and purity of these drug sources. Packaged Type A 
medicated articles and Type B medicated feeds shall be stored in 
designated areas in their original closed containers. Bulk Type A 
medicated articles and bulk Type B medicated feeds shall be identified 
and stored in a manner such that their identity, strength, quality, and 
purity will be maintained. All Type A medicated articles and Type B 
medicated feeds shall be used in accordance with their labeled mixing 
directions.