[Federal Register Volume 64, Number 213 (Thursday, November 4, 1999)]
[Notices]
[Pages 60226-60227]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-28866]


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DEPARTMENMT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated June 22, 1999, and published in the Federal 
Register on June 29, 1999, (64 FR 3425), Chiragene, Inc., 7 Powder Horn 
Drive, Warren, New Jersey 07059, 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
------------------------------------------------------------------------
N-Ethylamphetamine (1475)...................  I
2,5-Dimethoxyamphetamine (7396).............  I
3,4-Methylenedioxyamphetamine (7400)........  I
4-Methoxyamphetamine (7411).................  I
Amphetamine (1100)..........................  II
Methylphenidate (1724)......................  II
------------------------------------------------------------------------

    The firm plans to manufacture the listed controlled substance to 
supply their customers.
    No comments or objections have been received. DEA has considered 
the factors in Title 21, United States Code, Section 832(a) and 
determined that the registration of Chiragene, Inc. to manufacture the 
listed controlled substances is consistent with the public interest at 
this time. DEA has investigated Chiragene, 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

[[Page 60227]]

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: October 25, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Controls, Drug 
Enforcement Administration.
[FR Doc. 99-28866 Filed 11-3-99; 8:45 am]
BILLING CODE 4410-09-M