Manufacturer of Controlled Substances; Notice of Application, 25375 [2011-10853]
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Federal Register / Vol. 76, No. 86 / Wesnesday, May 4, 2011 / Notices
Therefore, pursuant to 21 U.S.C. 952(a)
and 958(a), and in accordance with 21
CFR 1301.34, the above named company
is granted registration as an importer of
the basic classes of controlled
substances listed.
DEPARTMENT OF JUSTICE
Dated: April 26, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
25375
By Notice dated November 19, 2010,
and published in the Federal Register
on December 3, 2010, 75 FR 75496,
Tocris Cookson, Inc., 16144 Westwoods
Business Park, Ellisville, Missouri
63021–4500, made application by
renewal to the Drug Enforcement
[FR Doc. 2011–10863 Filed 5–3–11; 8:45 am]
BILLING CODE 4410–09–P
Administration (DEA) to be registered as
an importer of the following basic
classes of controlled substances:
Drug Enforcement Administration
Importer of Controlled Substances;
Notice of Registration
Drug
Schedule
jlentini on DSKJ8SOYB1PROD with NOTICES
Marihuana (7360) ................................................................................................................................................................................
Tetrahydrocannabinols (7370) .............................................................................................................................................................
4-Bromo-2,5-dimethoxyamphetamine (7391) ......................................................................................................................................
3,4-Methylenedioxymethamphetamine (7405) ....................................................................................................................................
Amphetamine (1100) ...........................................................................................................................................................................
Phencyclidine (7471) ...........................................................................................................................................................................
Cocaine (9041) ....................................................................................................................................................................................
Diprenorphine (9058) ...........................................................................................................................................................................
Fentanyl (9801) ....................................................................................................................................................................................
The company plans to import small
quantities of the above-listed controlled
substances for distribution to its
customers for non-clinical, laboratorybased research only.
In reference to drug code 7360
(Marihuana), the company plans to
import synthetic cannabinoid agonists.
In reference to drug code 7370
(Tetrahydrocannabinols), the company
will import a synthetic Delta-9-THC. No
other activity for these drug codes are
authorized for this registration.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and 952(a),
and determined that the registration of
Tocris Cookson, Inc. to import the basic
classes of controlled substances is
consistent with the public interest and
with United States obligations under
international treaties, conventions, or
protocols in effect on May 1, 1971. DEA
has investigated Tocris Cookson, Inc. to
ensure that the company’s registration is
consistent with the public interest. The
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. 952(a)
and 958(a), and in accordance with 21
CFR 1301.34, the above named company
is granted registration as an importer of
the basic classes of controlled
substances listed.
VerDate Mar<15>2010
17:45 May 03, 2011
Jkt 223001
Dated: April 26, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
for conversion and sale to dosage form
manufacturers.
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 should be addressed, in
quintuplicate, to the Drug Enforcement
Administration, Office of Diversion
Control, Federal Register Representative
(ODL), 8701 Morrissette Drive,
Springfield, Virginia 22152; and must be
filed no later than July 5, 2011.
[FR Doc. 2011–10864 Filed 5–3–11; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Application
Pursuant to § 1301.33(a) Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on February 9, 2011,
Rhodes Technologies, 498 Washington
Street, Coventry, Rhode Island 02816,
made application by renewal to the
Drug Enforcement Administration
(DEA) to be registered as a bulk
manufacturer of the following basic
classes of controlled substances:
Drug
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[FR Doc. 2011–10853 Filed 5–3–11; 8:45 am]
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The company plans to manufacture
the listed controlled substances in bulk
PO 00000
Dated: April 25, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
Schedule
Tetrahydrocannabinols (7370) ......
Methylphenidate (1724) ................
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Hydrocodone (9193) .....................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Oxymorphone (9652) ....................
Noroxymorphone (9668) ...............
Fentanyl (9801) ............................
Sfmt 4703
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Application
Pursuant to § 1301.33(a) Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on February 15, 2011,
Siemens Healthcare Diagnostics Inc.,
Attn: RA, 100 GBC Drive, Mail Stop 514,
Newark, Delaware 19702, made
application by renewal to the Drug
Enforcement Administration (DEA) to
be registered as a bulk manufacturer of
E:\FR\FM\04MYN1.SGM
04MYN1
]]>Agencies
[Federal Register Volume 76, Number 86 (Wednesday, May 4, 2011)]
[Notices]
[Page 25375]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-10853]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a) Title 21 of the Code of Federal
Regulations (CFR), this is notice that on February 9, 2011, Rhodes
Technologies, 498 Washington Street, Coventry, Rhode Island 02816, made
application by renewal to the Drug Enforcement Administration (DEA) to
be registered as a bulk manufacturer of the following basic classes of
controlled substances:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)................................. I
Methylphenidate (1724)....................................... II
Codeine (9050)............................................... II
Dihydrocodeine (9120)........................................ II
Oxycodone (9143)............................................. II
Hydromorphone (9150)......................................... II
Hydrocodone (9193)........................................... II
Oripavine (9330)............................................. II
Thebaine (9333).............................................. II
Oxymorphone (9652)........................................... II
Noroxymorphone (9668)........................................ II
Fentanyl (9801).............................................. II
------------------------------------------------------------------------
The company plans to manufacture the listed controlled substances
in bulk for conversion and sale to dosage form manufacturers.
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 should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than July 5, 2011.
Dated: April 25, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-10853 Filed 5-3-11; 8:45 am]
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