[Federal Register Volume 64, Number 129 (Wednesday, July 7, 1999)]
[Notices]
[Page 36717]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-17094]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Registration

    By Notice dated February 23, 1999, and published in the Federal 
Register on March 5, 1999, (64 FR 10724), 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
------------------------------------------------------------------------
Methylphenide (1724).......................  II
Amobarbital (2125).........................  II
Pentobarbital (2270).......................  II
Secobarbital (2315)........................  II
Glutethimide (2550)........................  II
Methadone (9250)...........................  II
Methadone-intermediate (9254)..............  II
Dextropropoxphene, 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 21 U.S.C. 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: June 23, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-17094 Filed 7-6-99; 8:45 am]
BILLING CODE 4410-09-M