[Code of Federal Regulations]
[Title 16, Volume 2]
[Revised as of January 1, 2004]
From the U.S. Government Printing Office via GPO Access
[CITE: 16CFR1702.16]

[Page 756]
 
                     TITLE 16--COMMERCIAL PRACTICES
 
             CHAPTER II--CONSUMER PRODUCT SAFETY COMMISSION
 
PART 1702--PETITIONS FOR EXEMPTIONS FROM POISON PREVENTION PACKAGING 
ACT REQUIREMENTS; PETITION PROCEDURES AND REQUIREMENTS--Table of Contents
 
Sec.  1702.16  Petitions requesting an exemption for a drug or a new drug.

    (a) Where the petition requests an exemption for a drug, as defined 
in section 201(g)(1) of the Federal Food, Drug, and Cosmetic Act (21 
U.S.C. 321(g)(1), the petitioner shall include those reports required to 
be filed under the Food and Drug Administration's Adverse Reaction 
Reporting Program.
    (b) [Reserved]

[45 FR 13064, Feb. 28, 1980, as amended at 66 FR 40115, Aug. 2, 2001]