[Federal Register Volume 64, Number 200 (Monday, October 18, 1999)]
[Notices]
[Page 56225]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-27099]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on August 12, 1999, Cedarburg 
Laboratories, Inc., 870 Bandger Circle, Grafton, Wisconsin 53024, made 
application by letter to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of propiram (9649), a basic class 
of controlled substance listed in Schedule I.
    the firm plans will manufacture propiram in the process of 
manufacturing other targeted test compounds for another firm.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substance may file comments or objections 
to the issuance of the proposed registration.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than December 17, 1999.

    Dated: October 8, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-27099 Filed 10-15-99; 8:45 am]
BILLING CODE 4410-09-M