Manufacturer of Controlled Substances; Notice of Registration; American Radiolabeled Chemicals, Inc., 49547-49548 [2013-19619]
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49547
Federal Register / Vol. 78, No. 157 / Wednesday, August 14, 2013 / Notices
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a), and
determined that the registration of
Wildlife Laboratories, Inc., to
manufacture the listed basic class of
controlled substance is consistent with
the public interest at this time. DEA has
investigated Wildlife Laboratories, 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.
823(a), and in accordance with 21 CFR
1301.33, the above named company is
granted registration as a bulk
manufacturer of the basic class of
controlled substance listed.
Dated: August 5, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
factors in 21 U.S.C. 823(a) and
determined that the registration of
Penick Corporation to manufacture the
listed basic classes of controlled
substances is consistent with the public
interest at this time.
DEA has investigated Penick
Corporation 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.
823(a), and in accordance with 21 CFR
1301.33, the above named company is
granted registration as a bulk
manufacturer of the basic classes of
controlled substances listed.
Dated: August 5, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2013–19614 Filed 8–13–13; 8:45 am]
BILLING CODE 4410–09–P
Dated: August 5, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
BILLING CODE 4410–09–P
[FR Doc. 2013–19612 Filed 8–13–13; 8:45 am]
[FR Doc. 2013–19608 Filed 8–13–13; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Registration;
Penick Corporation
Manufacturer of Controlled
Substances, Notice of Registration,
Rhodes Technologies
By Notice dated April 10, 2013, and
published in the Federal Register on
April 19, 2013, 78 FR 23595, Penick
Corporation, 33 Industrial Park Road,
Pennsville, New Jersey 08070, 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:
By Notice dated April 10, 2013, and
published in the Federal Register on
April 19, 2013, 78 FR 23596, 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 basic classes of controlled
substances:
tkelley on DSK3SPTVN1PROD with NOTICES
Drug
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The company plans to manufacture
the listed controlled substances as bulk
controlled substance intermediates for
distribution to its customers.
No comments or objections have been
received. DEA has considered the
16:16 Aug 13, 2013
Drug
Schedule
Cocaine (9041) .............................
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Ecgonine (9180) ...........................
Hydrocodone (9193) .....................
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Oxymorphone (9652) ...................
VerDate Mar<15>2010
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and
determined that the registration of
Rhodes Technologies to manufacture
the listed basic classes of controlled
substances is consistent with the public
interest at this time. DEA has
investigated Rhodes Technologies 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.
823(a), and in accordance with 21 CFR
1301.33, the above named company is
granted registration as a bulk
manufacturer of the basic classes of
controlled substances listed.
Jkt 229001
DEPARTMENT OF JUSTICE
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The company plans to manufacture
the listed controlled substances in bulk
for conversion and sale to dosage form
manufacturers.
Frm 00104
Fmt 4703
Manufacturer of Controlled
Substances; Notice of Registration;
American Radiolabeled Chemicals, Inc.
By Notice dated April 10, 2013, and
published in the Federal Register on
April 19, 2013, 78 FR 23596, American
Radiolabeled Chemicals, Inc., 101 Arc
Drive, St. Louis, Missouri 63146, 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:
Schedule
Tetrahydrocannabinols (7370) .....
Methylphenidate (1724) ................
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Hydrocodone (9193) .....................
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Oxymorphone (9652) ...................
Noroxymorphone (9668) ..............
Fentanyl (9801) ............................
PO 00000
Drug Enforcement Administration
Sfmt 4703
Drug
Gamma
Hydroxybutyric
Acid
(2010).
Ibogaine (7260) ............................
Lysergic acid diethylamide (7315)
Tetrahydrocannabinols (7370) .....
Dimethyltryptamine (7435) ...........
1-[1-(2Thienyl)cyclohexyl]piperidine
(7470).
Dihydromorphine (9145) ...............
Heroin (9200) ...............................
Normorphine (9313) .....................
Amphetamine (1100) ....................
Methamphetamine (1105) ............
Amobarbital (2125) .......................
Phencyclidine (7471) ....................
Phenylacetone (8501) ..................
Cocaine (9041) .............................
E:\FR\FM\14AUN1.SGM
14AUN1
Schedule
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49548
Federal Register / Vol. 78, No. 157 / Wednesday, August 14, 2013 / Notices
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Ecgonine (9180) ...........................
Hydrocodone (9193) .....................
Meperidine (9230) ........................
Metazocine (9240) ........................
Dextropropoxyphene, bulk (nondosage forms) (9273).
Morphine (9300) ...........................
Oripavine (9330) ...........................
Thebaine (9333) ...........................
Oxymorphone (9652) ...................
Phenazocine (9715) .....................
Carfentanil (9743) .........................
Fentanyl (9801) ............................
ACTION:
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SUMMARY:
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The company plans to manufacture
small quantities of the listed controlled
substances as radiolabeled compounds
for biochemical research.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. § 823(a) and
determined that the registration of
American Radiolabeled Chemicals, Inc.,
to manufacture the listed basic classes
of controlled substances is consistent
with the public interest at this time.
DEA has investigated American
Radiolabeled Chemicals, 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. 823(a),
and in accordance with 21 CFR
§ 1301.33, the above named company is
granted registration as a bulk
manufacturer of the basic classes of
controlled substances listed.
Dated: August 5, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2013–19619 Filed 8–13–13; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
tkelley on DSK3SPTVN1PROD with NOTICES
Employment and Training
Administration
Comment Request for Information
Collection for Job Corps Application
Data (Job Corps Enrollee Allotment
Determination, Extension Without
Revisions)
Employment and Training
Administration (ETA), Labor.
AGENCY:
VerDate Mar<15>2010
16:16 Aug 13, 2013
Notice.
Schedule
Drug
Jkt 229001
The Department of Labor, as
part of its continuing effort to reduce
paperwork and respondent burden,
conducts a pre-clearance consultation
program to provide the general public
and federal agencies with an
opportunity to comment on proposed
and/or continuing collection of
information in accordance with the
Paperwork Reduction Act of 1995
(PRA95) [44 U.S.C. 3506(c)(2)(A)].
This program helps to ensure that
requested data can be provided in the
desired format, reporting burden (time
and financial resources) is minimized,
collection instruments are clearly
understood, and the impact of collection
requirements on respondents can be
properly assessed. Currently, ETA is
soliciting comments regarding the
collection of data about OMB 1205–
0030 (January 31, 2014).
DATES: Written comments must be
submitted to the office listed in the
addressee’s section below on or before
October 15, 2013.
ADDRESSES: Submit written comments
to Linda Estep, Office of Job Corps
Room N4507 Employment and Training
Administration, 200 Constitution
Avenue NW., Washington, DC 20210.
Telephone number: 888–886–1303 ext.
7212 (this is a toll-free number). Fax:
202–693–2764; email:
estep.linda@dol.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Job Corps is the nation’s largest
residential educational and career
technical training program for young
Americans. Job Corps was established in
1964 by the Economic Opportunity Act,
and currently is authorized by Title I–
C of the Workforce Investment Act of
1998. For almost 50 years, Job Corps has
helped prepare nearly three million atrisk young people, ages 16 to 24, for
success in our nation’s workforce. With
125 centers in 48 states, Puerto Rico,
and the District of Columbia, Job Corps
assists students across the nation in
attaining academic credentials,
including a High School Diploma (HSD)
and/or General Educational
Development (GED), and career
technical training credentials, including
industry-recognized certifications, state
licensures, and pre-apprenticeship
credentials.
Job Corps is administered by the U.S.
Department of Labor (DOL) through the
Office of Job Corps and six Regional
Offices. DOL awards and administers
contracts for the recruiting and
screening of new students, center
PO 00000
Frm 00105
Fmt 4703
Sfmt 4703
operations, and the placement and
transitional support of graduates and
former enrollees. Large and small
corporations and nonprofit
organizations manage and operate 97
Job Corps centers under contractual
agreements with DOL.
These contract Center Operators are
selected through a competitive
procurement process that evaluates
potential operators’ technical expertise,
proposed costs, past performance, and
other factors, in accordance with the
Competition in Contracting Act and the
Federal Acquisition Regulations. The
remaining 28 Job Corps centers, called
Civilian Conservation Centers, are
operated by the U.S. Department of
Agriculture Forest Service, via an
interagency agreement. The DOL has a
direct role in the operation of Job Corps,
and does not serve as a pass-through
agency for this program.
II. Review Focus
The Department of Labor is
particularly interested in comments
which:
• Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
agency’s functions, including whether
the information has practical utility;
• Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
• Enhance the quality, utility, and
clarity of the information to be
collected; and
• Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
III. Current Actions
Type of Review: Extension without
changes.
Title: Job Corps Enrollee Allotment
Determination.
OMB Number: Existing number OMB
1205–0030.
Affected Public: Individuals or
households, Federal Government.
Form(s): ETA 658.
Total Annual Responses: 1,749.
Average Time per Response: 3
minutes.
Estimated Total Annual Burden
Hours: 87.5 hours.
Total Annual Burden Cost for
Respondents: $450.62.
The purpose of this collection is to
provide a vehicle to make allotments
E:\FR\FM\14AUN1.SGM
14AUN1
]]>Agencies
[Federal Register Volume 78, Number 157 (Wednesday, August 14, 2013)]
[Notices]
[Pages 49547-49548]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-19619]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration;
American Radiolabeled Chemicals, Inc.
By Notice dated April 10, 2013, and published in the Federal
Register on April 19, 2013, 78 FR 23596, American Radiolabeled
Chemicals, Inc., 101 Arc Drive, St. Louis, Missouri 63146, 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
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid (2010)........... I
Ibogaine (7260)............................ I
Lysergic acid diethylamide (7315).......... I
Tetrahydrocannabinols (7370)............... I
Dimethyltryptamine (7435).................. I
1-[1-(2-Thienyl)cyclohexyl]piperidine I
(7470).
Dihydromorphine (9145)..................... I
Heroin (9200).............................. I
Normorphine (9313)......................... I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Amobarbital (2125)......................... II
Phencyclidine (7471)....................... II
Phenylacetone (8501)....................... II
Cocaine (9041)............................. II
[[Page 49548]]
Codeine (9050)............................. II
Dihydrocodeine (9120)...................... II
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Ecgonine (9180)............................ II
Hydrocodone (9193)......................... II
Meperidine (9230).......................... II
Metazocine (9240).......................... II
Dextropropoxyphene, bulk (non-dosage forms) II
(9273).
Morphine (9300)............................ II
Oripavine (9330)........................... II
Thebaine (9333)............................ II
Oxymorphone (9652)......................... II
Phenazocine (9715)......................... II
Carfentanil (9743)......................... II
Fentanyl (9801)............................ II
------------------------------------------------------------------------
The company plans to manufacture small quantities of the listed
controlled substances as radiolabeled compounds for biochemical
research.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. Sec. 823(a) and determined that the
registration of American Radiolabeled Chemicals, Inc., to manufacture
the listed basic classes of controlled substances is consistent with
the public interest at this time. DEA has investigated American
Radiolabeled Chemicals, 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. 823(a), and in accordance with 21 CFR Sec. 1301.33, the
above named company is granted registration as a bulk manufacturer of
the basic classes of controlled substances listed.
Dated: August 5, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2013-19619 Filed 8-13-13; 8:45 am]
BILLING CODE 4410-09-P
