[Federal Register Volume 76, Number 195 (Friday, October 7, 2011)]
[Notices]
[Page 62449]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-26063]


-----------------------------------------------------------------------

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 August 9, 2011, Johnson 
Matthey, Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, 
West Deptford, New Jersey 08066-1742, made application by letter to the 
Drug Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of Diphenoxylate (9170), a basic class of controlled 
substance listed in schedule II.
    The company plans to manufacture the listed controlled substance 
for sale in bulk to its customers for formulation into finished 
pharmaceuticals.
    Any other such applicant, and any person who is presently 
registered with DEA to manufacture such substance, 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 December 6, 2011.

    Dated: September 28, 2011.
 Joseph T. Rannazzisi,
 Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2011-26063 Filed 10-6-11; 8:45 am]
BILLING CODE 4410-09-P