[Federal Register Volume 69, Number 32 (Wednesday, February 18, 2004)]
[Notices]
[Pages 7655-7656]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-3482]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By notices dated March 11, 2003, and published in the Federal 
Register on April 2, 2003 (68 FR 16088), dated April 3, 2003, and 
published in the Federal Register on April 15, 2003 (68 FR 18262), 
dated June 20, 2003, and published in the Federal Register on July 8, 
2003 (68 FR 40686), and dated October 7, 2003, and published in the 
Federal Register on October 29, 2003 (68 FR 61698), Cody Laboratories, 
Inc., 331 33rd Street, Cody, Wyoming 82414, made application by letters 
and by renewals to the Drug Enforcement Administration for registration 
as a bulk manufacturer of the basic classes of controlled substances 
listed below:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Dihydromorphine (9145)......................  I
Amphetamine (1100)..........................  II
Methamphetamine (1105)......................  II
Amobarbital (2125)..........................  II
Pentobarbital (2270)........................  II
Secobarbital (2315).........................  II
Phenylacetone (8501)........................  II
Oxycodone (9143)............................  II
Hydromorphone (9150)........................  II
Diphenoxylate (9170)........................  II
Meperidine (9230)...........................  II
Oxymorphone (9652)..........................  II
Sufentanil (9740)...........................  II
Fentanyl (9801).............................  II
------------------------------------------------------------------------

    On December 30, 2003, the firm requested that their registration be 
modified to reflect an address change to 601 Yellowstone Drive, Cody, 
Wyoming 82414. That modification was effected on January 8, 2004.
    The firm plans to manufacture bulk materials for distribution to 
its customers.
    No comments or objections have been received. DEA has considered 
the factors in title 21, United States Code, section 823(a) and 
determined that the registration of Cody Laboratories, Inc. to 
manufacture the listed controlled substances is consistent with the 
public

[[Page 7656]]

interest at this time. DEA has investigated Cody Laboratories, Inc. to 
ensure that the company's registration is consistent with the public 
interest. This 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 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 is granted.

    Dated: February 4, 2004.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-3482 Filed 2-17-04; 8:45 am]
BILLING CODE 4410-09-M