[Federal Register: March 4, 2005 (Volume 70, Number 42)]
[Notices]
[Page 10679]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04mr05-108]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to section 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on November 11, 2004, JFC
Technologies, LLC, 100 West Main Street, Bound Brook, New Jersey 08805,
made application by renewal to the Drug Enforcement Administration
(DEA) for registration as a bulk manufacturer of the basic class of
controlled substances listed in Schedule II:
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Drug Schedule
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Diphenozylate (9170)........................ II
Hydrocodone (9193).......................... II
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The company plans to manufacture the listed controlled substances
in bulk for distribution to its customers.
Any other such applicant and any person who is presently registered
with DEA to manufacture such substances may file comments or objections
to the issuance of the proposed registration pursuant to 21 CFR
1301.33(a).
Any such written comments or objections being sent via regular mail
may be addressed, in quintuplicate, to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537, Attention: DEA Federal Register
Representative, Liaison and Policy Section (ODL); or any being sent via
express mail should be sent to DEA Headquarters, Attention: DEA Federal
Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria,
Virginia 22301; and must be filed no later than May 3, 2005.
Dated: February 23, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-4227 Filed 3-3-05; 8:45 am]
BILLING CODE 4410-09-P