Manufacturer of Controlled Substances; Notice of Application, 15219 [E6-4351]
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Federal Register / Vol. 71, No. 58 / Monday, March 27, 2006 / Notices
6(a) of the National Cooperative
Research and Production Act of 1993,
15 U.S.C. 4301 et seq. (‘‘the Act’’), Open
SystemC Initiative (‘‘OSCI’’) has filed
written notifications simultaneously
with the Attorney General and the
Federal Trade Commission disclosing
changes in its membership. The
notifications were filed for the purpose
of extending the Act’s provisions
limiting the recovery of antitrust
plaintiffs to actual damages under
specified circumstances. Specifically,
Bluespec. Inc., Waltham, MA; Canon
Inc., Tokyo, Japan; Carbon Design
Systems, Waltham, MA; Doulos Ltd.,
Ringwood, Hampshire, United
Kingdom, GreenSocs Ltd., Cambridge,
United Kingdom; Jeda Technologies,
Inc., Los Altos, CA; and Tenison
Technology EDA Ltd., Cambridge,
United Kingdom have been added as
parties to this venture. Also, NEC
Electronics, Inc., Santa Clara, CA;
Panasonic, Secaucus, NJ; and Verisity
Design, Inc., Mountain View, CA have
withdrawn as parties to this venture.
No other changes have been made in
either the membership or planned
activity of the group research project.
Membership in this group research
project remains open, and OSCI intends
to file additional written notification
disclosing all changes in membership.
On October 9, 2001, OSCI filed its
original notification pursuant to Section
6(a) of the Act. The Department of
Justice published a notice in the Federal
Register pursuant to Section 6(b) of the
Act on January 3, 2002 (67 FR 350).
The last notification was filed with
the Department on May 9, 2005. A
notice was published in the Federal
Register pursuant to section 6(b) of the
Act on June 3, 2005 (70 FR 32654).
Dorothy B. Fountain,
Deputy Director of Operations, Antitrust
Division.
[FR Doc. 06–2925 Filed 3–24–06; 8:45 am]
Administration (DEA) as a bulk
manufacturer of the basic classes of
controlled substances listed in Schedule
I and II:
Drug
Schedule
Marihuana (7360) .........................
Tetrahydrocannabinols (7370) .....
Amphetamine (1100) ....................
Methylphenidate (1724) ................
Pentobarbital (2270) .....................
Hydrocodone (9193) .....................
Meperidine(9230) .........................
Dextropropoxyphene (9273) .........
Fentanyl (9801) ............................
I
I
II
II
II
II
II
II
II
The company plans to manufacture
bulk controlled substances for use in
product development and for
distribution to its customers. In
reference to drug code 7360
(Marihuana), the company plans to bulk
manufacture cannabindiol as a synthetic
intermediate. This controlled substance
will be further synthesized to bulk
manufacture a synthetic THC (7370). No
other activity for this drug code is
authorized for this registration.
Any other such applicant and any
person who is presently registered with
DEA to manufacture such a substance
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 1, 2006.
Dated: March 20, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. E6–4351 Filed 3–24–06; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
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NATIONAL SCIENCE FOUNDATION
Advisory Committee for Environmental
Research and Education; Notice of
Meeting
In accordance with the Federal
Advisory Committee Act (Pub. L. 92–
463, as amended), the National Science
Foundation announces the following
meeting:
PO 00000
Frm 00063
Fmt 4703
Name: Advisory Committee for
Environmental Research and education
(9487).
Dates: April 12, 2006, 8:30 a.m.–5
p.m. and April 13, 2006, 8:30 a.m.–3:30
p.m.
Place: Stafford I, Room 1235, National
Science Foundation, 4201 Wilson Blvd.,
Arlington, Virginia 22230.
Type of Meeting: Open.
Contact Person: Melissa Lane,
Directorate for Geosciences, National
Science Foundation, Suite 705, 4201
Wilson Blvd, Arlington, Virginia 22230.
Phone 703–292–8500.
Minutes: May be obtained from the
contact person listed above.
Purpose of Meeting: To provide
advice, recommendations, and oversight
concerning support for environmental
research and education.
Agenda
April 12
Update on recent NSF environmental
activities.
Discussion of Observatory Workshop
Report.
Report by Director of OCI on
Environmental Cyberinfrastructure.
Report on NSF Strategic Plan
Development.
AC–ERE task group meetings.
Presentation on the NAS International
Human Dimensions of Global
Change committee.
April 13
AC–ERE task group reports.
AC–ERE Advice on Development of
Water Initiative.
International Polar Year Update.
Future of Dynamics of Coupled
Natural and Human System
Program.
Discussion of Engineering themes on
environment and sustainability.
Meeting with the Director.
Dated: March 21, 2006.
Susanne Bolton,
Committee Management Officer.
[FR Doc. 06–2897 Filed 3–24–06; 8:45 am]
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NATIONAL SCIENCE FOUNDATION
Proposal Review Panel for Materials
Research; Notice of Meeting
BILLING CODE 4410–09–P
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 10,
2005, Organichem Corporation, 33
Riverside Avenue, Rensselaer, New
York 12144, made application by
renewal, and by letter on December 12,
2005, requesting the addition of
Marihuana (7360) to their registration
with the Drug Enforcement
15219
Sfmt 4703
In accordance with the Federal
Advisory Committee Act (Pub. L. 92–
463 as amended), the National Science
Foundation announces the following
meeting:
Name: Proposal Review Panel for
Materials Research (DMR) #1203
Dates & Times: May 16, 2006; 7:30
a.m.–9 p.m.; May 17, 2006; 8 a.m.–4p.m.
Place: University of Nebraska,
Lincoln, NE.
\\ALPHA3\E\FR\FM\27MRN1.SGM
27MRN1
Agencies
[Federal Register Volume 71, Number 58 (Monday, March 27, 2006)]
[Notices]
[Page 15219]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-4351]
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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 10, 2005, Organichem
Corporation, 33 Riverside Avenue, Rensselaer, New York 12144, made
application by renewal, and by letter on December 12, 2005, requesting
the addition of Marihuana (7360) to their registration with the Drug
Enforcement Administration (DEA) as a bulk manufacturer of the basic
classes of controlled substances listed in Schedule I and II:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Marihuana (7360)........................... I
Tetrahydrocannabinols (7370)............... I
Amphetamine (1100)......................... II
Methylphenidate (1724)..................... II
Pentobarbital (2270)....................... II
Hydrocodone (9193)......................... II
Meperidine(9230)........................... II
Dextropropoxyphene (9273).................. II
Fentanyl (9801)............................ II
------------------------------------------------------------------------
The company plans to manufacture bulk controlled substances for use
in product development and for distribution to its customers. In
reference to drug code 7360 (Marihuana), the company plans to bulk
manufacture cannabindiol as a synthetic intermediate. This controlled
substance will be further synthesized to bulk manufacture a synthetic
THC (7370). No other activity for this drug code is authorized for this
registration.
Any other such applicant and any person who is presently registered
with DEA to manufacture such a substance may file comments or
objections to the issuance of the proposed registration pursuant to 21
CFR Sec. 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 1, 2006.
Dated: March 20, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E6-4351 Filed 3-24-06; 8:45 am]
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