[Federal Register: December 27, 2007 (Volume 72, Number 247)]
[Notices]
[Page 73361]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27de07-80]
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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 November 15, 2007, Organix
Inc., 240 Salem Street, Woburn, Massachusetts 01801, made application
by renewal to the Drug Enforcement Administration (DEA) to be
registered as a bulk manufacturer of the basic classes of controlled
substances listed in schedule I and II:
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Drug Schedule
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Tetrahydrocannabinols (7370)............... I
Cocaine (9041)............................. II
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The company plans to manufacture the listed controlled substances
in bulk for sale to its customers for research purposes.
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
should be addressed, in quintuplicate, to the Drug Enforcement
Administration, Office of Diversion Control, Federal Register
Representative (ODL), Washington, DC 20537, or any being sent via
express mail should be sent to Drug Enforcement Administration, Office
of Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than February 25, 2008.
Dated: December 17, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E7-25114 Filed 12-26-07; 8:45 am]
BILLING CODE 4410-09-P