[Federal Register Volume 75, Number 232 (Friday, December 3, 2010)]
[Notices]
[Page 75497]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2010-30351]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec.  1301.33(a), Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on October 29, 2010, Siegfried 
(USA), Inc., 33 Industrial Park Road, Pennsville, New Jersey 08070, 
made application by letter to the Drug Enforcement Administration (DEA) 
to be registered as a bulk manufacturer of Hydromorphinol (9301), a 
basic class of controlled substance listed in schedule I.
    The company plans to manufacture small quantities of the listed 
controlled substance in bulk for distribution to its customers for use 
as reference standards.
    Any other such applicant, and any person who is presently 
registered with DEA to manufacture such substances, may file comments 
or objections to the issuance of the proposed registration pursuant to 
21 CFR 1301.33(a).
    Any such written comments or objections should be addressed, in 
quintuplicate, to the Drug Enforcement Administration, Office of 
Diversion Control, Federal Register Representative (ODL), 8701 
Morrissette Drive, Springfield, Virginia 22152; and must be filed no 
later than February 1, 2011.

    Dated: November 19, 2010.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2010-30351 Filed 12-2-10; 8:45 am]
BILLING CODE 4410-09-P