[Federal Register Volume 63, Number 196 (Friday, October 9, 1998)]
[Notices]
[Page 54492]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-27104]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on September 2, 1998, Johnson 
Matthey, Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, 
West Deptford, New Jersey 08066, made application by letter to the Drug 
Enforcement Administration (DEA) for registration as a bulk 
manufacturer of methamphetamine (1105), a basic class of controlled 
substance listed in Schedule II.
    The firm plans to manufacture methamphetamine in bulk form for 
distribution to finished dosage manufacturers.
    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.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than December 8, 1998.

    Dated: October 1, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-27104 Filed 10-8-98; 8:45 am]
BILLING CODE 4410-09-M