[Federal Register Volume 65, Number 111 (Thursday, June 8, 2000)]
[Notices]
[Page 36466]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 00-14478]


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

DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated February 10, 2000, and published in the Federal 
Register on February 17, 2000, (65 FR 33) Ganes Chemicals Inc., 
Industrial Park Road, Pennsville, New Jersey 08070, made application by 
renewal to the Drug Enforcement Administration (DEA) to be registered 
as a bulk manufacturer of the basic classes of controlled substances 
listed below:

------------------------------------------------------------------------
                   Drug                               Schedule
------------------------------------------------------------------------
Methylphenidate (1724)....................  II
Amobarbital (2125)........................  II
Pentobarbital (2270)......................  II
Secobarbital (2315).......................  II
Glutethimide (2550).......................  II
Methadone (9250)..........................  II
Methadone-intermediate (9254).............  II
Dextropopoxyphene, bulk (non-dosage forms)  II
 (9273).
------------------------------------------------------------------------

    The firm plans to manufacture the listed controlled substances for 
distribution as bulk products to its customers.
    DEA has considered the factors in Title 21, United States Code, 
Section 823(a) and determined that the registration of Ganes Chemicals, 
Inc. to manufacture the listed controlled substances is consistent with 
the public interest at this time. DEA has investigated Ganes Chemicals, 
Inc. on a regular basis to ensure that the company's continued 
registration is consistent with the public interest. These 
investigations have included inspection and testing of the company's 
physical security systems, audits of the company's records, 
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 28 CFR 0.100 and 0.104, the Deputy Assistant 
Administrator, Office of Diversion Control, hereby orders that the 
application submitted by the above firm for registration as a bulk 
manufacturer of the basic classes of controlled substances listed above 
is granted.

    Dated: May 25, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 00-14478 Filed 6-7-00; 8:45 am]
BILLING CODE 4410-09-M