[Federal Register Volume 65, Number 28 (Thursday, February 10, 2000)]
[Notices]
[Page 6633]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-3142]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated October 8, 1999, and published in the Federal 
Register on October 18, 1999, (64 FR 56225), Cedarburg Laboratories, 
Inc., 870 Badger Circle, Grafton, Wisconsin 53024, made application by 
letter to the Drug Enforcement Administration (DEA) to be registered as 
a bulk manufacturer of propiram (9649), a basic class of controlled 
substance listed in Schedule I.
    The firm will manufacture propiram in the process of manufacturing 
other targeted test compounds for another firm.
    DEA has considered the factors in Title 21, United States Code, 
Section 823(a) and determined that the registration of Cedarburg 
Laboratories, Inc. to manufacture propiram is consistent with the 
public interest at this time. DEA has investigated the company to 
ensure that the company's registration is coninspection 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 above is granted.

    Dated: February 4, 2000.
John H. King,
Deputy, Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 00-3142 Filed 2-9-00; 8:45 am]
BILLING CODE 4410-09-M