[Federal Register Volume 69, Number 92 (Wednesday, May 12, 2004)]
[Notices]
[Page 26407]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-10801]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated December 19, 2003, and published in the Federal 
Register on January 27, 2004, (69 FR 3946), Cambrex North Brunswick, 
Inc., Technology Center of New Jersey, 661 Highway One, North 
Brunswick, New Jersey 08902, made application by letter to the Drug 
Enforcement Administration for registration as a bulk manufacturer of 
Sufentanil (9740), a basic class of Schedule II controlled substance.
    The firm plans to manufacture Sufentanil to distribute in bulk 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 Cambrex North Brunswick, Inc. to 
manufacture the listed controlled substance is consistent with the 
public interest at this time. DEA has investigated Cambrex North 
Brunswick, 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 
class of controlled substance listed is granted.

    Dated: April 23, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-10801 Filed 5-11-04; 8:45 am]
BILLING CODE 4410-09-M