[Federal Register: August 10, 2004 (Volume 69, Number 153)]
[Notices]
[Page 48523]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr10au04-122]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated March 5, 2004, and published in the Federal
Register on March 15, 2004, (69 FR 12178), Johnson Matthey, Inc.,
Custom Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New
Jersey 08066, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of
Methamphetamine (1105), and Hydromorphone (9150), the basic classes of
controlled substances listed in Schedule II. The firm had inadvertently
dropped the two basic classes from its renewal application submitted on
August 25, 2003, and published in the Federal Register on February 18,
2004 (69 FR 7656).
The company plans to manufacture the listed controlled substances
in bulk to supply to its customers.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and determined that the registration of
Johnson Matthey, Inc., to manufacture the listed basic classes of
controlled substances is consistent with the public interest at this
time. DEA has investigated Johnson Matthey, Inc., to ensure that the
company's registration is consistent with the public interest. The
investigation has included inspection and testing of the company's
physical security systems, verification of the company's compliance
with state and local laws, and a review of the company's background and
history. Therefore, pursuant to 21 U.S.C. 823, and in accordance with
21 CFR 1301.33, the above named company is granted registration as a
bulk manufacturer of the basic classes of controlled substances listed.
Dated: July 28, 2004.
Joseph T. Rannazzisi,
Deputy Director, Office of Diversion Control, Drug Enforcement
Administration.
[FR Doc. 04-18174 Filed 8-9-04; 8:45 am]
BILLING CODE 4410-09-M