Manufacturer of Controlled Substances; Notice of Application, 73359 [E7-25053]
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73359
Federal Register / Vol. 72, No. 247 / Thursday, December 27, 2007 / Notices
DEPARTMENT OF JUSTICE
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Application
Importer of Controlled Substances;
Notice of Application
Pursuant to § 1301.33(a) of Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on May 31, 2007,
Innovacon, Inc., 4106 Sorrento Valley
Boulevard, San Diego, California 92121,
made application 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:
Pursuant to Title 21 Code of Federal
Regulations 1301.34(a), this is notice
that on November 7, 2007, Johnson
Matthey, Inc., Pharmaceutical Materials,
2003 Nolte Drive, West Deptford, New
Jersey 08066–1742, made application by
renewal to the Drug Enforcement
Administration (DEA) for registration as
an importer of the basic classes of
controlled substances listed in schedule
II:
Drug
Drug
Schedule
Tetrahydrocannabinols
(7370).
3,4–
Methylenedioxymethamphetamine (MDMA)
(7405).
Heroin (9200) ..................
Cocaine (9041) ...............
Hydromorphone (9150) ...
Hydrocodone (9193) .......
Levorphanol (9220) .........
Methadone (9250) ..........
Morphine (9300) .............
Thebaine (9333) .............
Phenylacetone (8501) ..................
Raw Opium (9600) .......................
Concentrate of Poppy Staw
(9670).
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mstockstill on PROD1PC66 with NOTICES
The company plans to utilize small
quantities of controlled substances to
produce drugs of abuse tests.
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. E7–25053 Filed 12–26–07; 8:45 am]
BILLING CODE 4410–09–P
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Schedule
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The company plans to import the
listed controlled substances as raw
materials for use in the manufacture of
bulk controlled substances for
distribution to its customers.
No comments, objections, or requests
for any hearings will be accepted on any
application for registration or reregistration to import crude opium,
poppy straw, concentrate of poppy
straw, or coca leaves.
Any bulk manufacturer who is
presently, or is applying to be,
registered with DEA to manufacture
such basic classes of controlled
substances listed in schedule I or II,
which fall under the authority of section
1002(a)(2)(B) of the Act (21 U.S.C.
952(a)(2)(B)) may, in the circumstances
set forth in 21 U.S.C. 958(i), file
comments or objections to the issuance
of the proposed registration and may, at
the same time, file a written request for
a hearing on such application pursuant
to 21 CFR 1301.43 and in such form as
prescribed by 21 CFR 1316.47.
Any such 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, VA 22152; and must
be filed no later than January 28, 2008.
This procedure is to be conducted
simultaneously with and independent
of the procedures described in 21 CFR
§ 1301.34(b), (c), (d), (e) and (f). As
noted in a previous notice published in
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the Federal Register on September 23,
1975, (40 FR 43745), all applicants for
registration to import a basic class of
any controlled substances in schedule I
or II are, and will continue to be,
required to demonstrate to the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, that the requirements
for such registration pursuant to 21
U.S.C. 958(a); 21 U.S.C. 823(a); and 21
CFR 1301.34(b), (c), (d), (e) and (f) are
satisfied.
Dated: December 18, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. E7–25043 Filed 12–26–07; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Application
Pursuant to § 1301.33(a) of Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on November 7, 2007,
Johnson Matthey, Inc., Custom
Pharmaceuticals Department, 2003
Nolte Drive, West Deptford, New Jersey
08066–1742, 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:
Drug
Tetrahydrocannabinols
(7370).
Dihydromorphine (9145)
Difenoxin (9168) .............
Propiram (9649) ..............
Amphetamine (1100) ......
Methamphetamine (1105)
Methylphenidate (1724) ..
Nabilone (7379) ..............
Cocaine (9041) ...............
Codeine (9050) ...............
Dihydrocodeine (9120) ...
Oxycodone (9143) ..........
Hydromorphone (9150) ...
Ecgonine (9180) .............
Hydrocodone (9193) .......
Meperidine (9230) ...........
Methadone (9250) ..........
Methadone intermediate
(9254).
Morphine (9300) .............
Thebaine (9333) .............
Oxymorphone (9652) ......
Noroxymorphone (9668)
Alfentanil (9737) ..............
Remifentanil (9739) ........
Sufentanil (9740) ............
Fentanyl (9801) ...............
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Agencies
[Federal Register Volume 72, Number 247 (Thursday, December 27, 2007)]
[Notices]
[Page 73359]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-25053]
[[Page 73359]]
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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 May 31, 2007, Innovacon,
Inc., 4106 Sorrento Valley Boulevard, San Diego, California 92121, made
application 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:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)............... I
3,4-Methylenedioxymethamphetamine (MDMA) I
(7405).
Heroin (9200).............................. I
Cocaine (9041)............................. II
Hydromorphone (9150)....................... II
Hydrocodone (9193)......................... II
Levorphanol (9220)......................... II
Methadone (9250)........................... II
Morphine (9300)............................ II
Thebaine (9333)............................ II
------------------------------------------------------------------------
The company plans to utilize small quantities of controlled
substances to produce drugs of abuse tests.
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. E7-25053 Filed 12-26-07; 8:45 am]
BILLING CODE 4410-09-P