[Federal Register Volume 77, Number 60 (Wednesday, March 28, 2012)]
[Rules and Regulations]
[Pages 18685-18686]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-7532]


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HEALTH AND HUMAN SERVICES DEPARTMENT

Food and Drug Administration

21 CFR Part 516


New Animal Drugs for Minor Use and Minor Species

CFR Correction

    In Title 21 of the Code of Federal Regulations, Parts 500 to 599, 
revised as of April 1, 2011, on page 96, in Sec.  516.20, (b)(2) is 
revised to read as follows:


Sec.  516.20  Content and format of a request for MUMS-drug 
designation.

* * * * *
    (b) * * *
    (2) The name and address of the sponsor; the name of the sponsor's 
primary contact person and/or permanent-resident U.S. agent including 
title, address, and telephone number; the established name (and 
proprietary name, if any) of the active pharmaceutical ingredient of 
the drug; and the name and address of the source

[[Page 18686]]

of the active pharmaceutical ingredient of the drug.
* * * * *
[FR Doc. 2012-7532 Filed 3-27-12; 8:45 am]
BILLING CODE 1505-01-D