Controlled Substances: 2014 Established Aggregate Production Quotas for Four Temporarily Controlled Synthetic Cannabinoids, 23376-23377 [2014-09556]
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23376
Federal Register / Vol. 79, No. 81 / Monday, April 28, 2014 / Notices
interest, and with United States
obligations under international treaties,
conventions, or protocols in effect on
May 1, 1971. DEA has investigated
Mylan Pharmaceuticals, 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.
Dated: April 21, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2014–09574 Filed 4–25–14; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Bulk Manufacturer of Controlled
Substances Application: Organix, Inc.
Notice of application with
opportunity for comment.
ACTION:
Registered bulk manufacturers of
the affected basic classes and applicants
therefore may file written comments or
objections to the issuance of the
proposed registration in accordance
with 21 CFR 1301.33(a) on or before
June 27, 2014.
ADDRESSES: Written comments should
be sent via regular or express mail to:
Drug Enforcement Administration,
Attention: DEA Federal Register
Representative/ODW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: The
Attorney General has delegated his
authority under the Controlled
DATES:
Controlled substance
Schedule
Gamma Hydroxybutyric Acid (2010) ...............................................
Lysergic acid diethylamide (7315) ..................................................
Heroin (9200) ..................................................................................
Morphine (9300) ..............................................................................
I ..............
I ..............
I ..............
II .............
The company plans to manufacture
reference standards for distribution to
its research and forensics customers.
Dated: April 21, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2014–09553 Filed 4–25–14; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
tkelley on DSK3SPTVN1PROD with NOTICES
Manufacturer of Controlled
Substances; Notice of Registration;
American Radiolabeled Chemicals, Inc.
By Notice dated December 16, 2013,
and published in the Federal Register
on January 2, 2014, 79 FR 151,
American Radiolabeled Chemicals, Inc.,
101 Arc Drive, St. Louis, Missouri
63146, made application by written
correspondence to the Drug
Enforcement Administration (DEA) to
be registered as a bulk manufacturer of
Methadone (9250), a basic class of
controlled substance listed in schedule
II.
The company plans to manufacture
small quantities of the listed controlled
VerDate Mar<15>2010
17:06 Apr 25, 2014
Jkt 232001
Narcotic/Nonnarcotic
nonnarcotic
nonnarcotic
narcotic
narcotic
substance as radiolabeled compounds
for biochemical research.
No comments or objections have been
received. The 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 class of
controlled substance is consistent with
the public interest at this time. The 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 class of
controlled substance listed.
PO 00000
Frm 00060
Fmt 4703
Substances Act to the Administrator of
the Drug Enforcement Administration
(DEA), 28 CFR 0.100(b). Authority to
exercise all necessary functions with
respect to the promulgation and
implementation of 21 CFR part 1301,
incident to the registration of
manufacturers, distributors, and
dispensers of controlled substances
(other than final orders in connection
with suspension, denial, or revocation
of registration) has been re-delegated to
the Deputy Assistant Administrator of
the DEA Office of Diversion Control
(‘‘Deputy Assistant Administrator’’)
pursuant to sec. 7(g) of 28 CFR part 0,
subpart R, App.
In accordance with 21 CFR
1301.33(a), this is notice that on
February 3, 2014, Organix, Inc., 240
Salem Street, Woburn, Massachusetts
01801, made application by written
correspondence to the DEA to be
registered as a bulk manufacturer of the
following basic classes of narcotic and
nonnarcotic controlled substances:
Sfmt 4703
Dated: April 21, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2014–09552 Filed 4–25–14; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–390]
Controlled Substances: 2014
Established Aggregate Production
Quotas for Four Temporarily
Controlled Synthetic Cannabinoids
Drug Enforcement
Administration (DEA), Department of
Justice.
ACTION: Notice.
AGENCY:
This notice establishes the
initial 2014 aggregate production quotas
for four temporarily controlled synthetic
cannabinoids: N-(1-amino-3,3-dimethyl1-oxobutan-2-yl)-1-pentyl-1H-indazole3-carboxamide (ADB–PINACA); N-(1amino-3-methyl-1-oxobutan-2-yl)-1-(4fluorobenzyl)-1H-indazole-3carboxamide (AB–FUBINACA);
SUMMARY:
E:\FR\FM\28APN1.SGM
28APN1
Federal Register / Vol. 79, No. 81 / Monday, April 28, 2014 / Notices
tkelley on DSK3SPTVN1PROD with NOTICES
quinolin-8-yl 1-(5-fluoropentyl)-1Hindole-3-carboxylate (5-fluoro-PB–22;
5F–PB–22); and quinolin-8-yl 1-pentyl1H-indole-3-carboxylate (PB–22;
QUPIC).
DATES: Effective April 28, 2014.
FOR FURTHER INFORMATION CONTACT:
Ruth A. Carter, Office of Diversion
Control, Drug Enforcement
Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia
22152, Telephone: (202) 598–6812.
SUPPLEMENTARY INFORMATION:
Background
Section 306 of the Controlled
Substances Act (CSA) (21 U.S.C. 826)
requires the Attorney General to
establish aggregate production quotas
for each basic class of controlled
substance listed in schedules I and II
and for the list I chemicals ephedrine,
pseudoephedrine, and
phenylpropanolamine. The Attorney
General has delegated this authority to
the Administrator of the DEA, 28 CFR
0.100, who in turn has redelegated that
authority to the Deputy Administrator of
the DEA, 28 CFR part 0, subpt. R, App.
On February 10, 2014, the DEA
published in the Federal Register a final
order to temporarily place four synthetic
cannabinoids, quinolin-8-yl 1-pentyl1H-indole-3-carboxylate (PB–22),
quinolin-8-yl 1-(5-fluoropentyl)-1Hindole-3-carboxylate (5F–PB–22), N-(1amino-3-methyl-1-oxobutan-2-yl)-1-(4fluorobenzyl)-1H-indazole-3carboxamide (AB–FUBINACA), and N(1-amino-3,3-dimethyl-1-oxobutan-2-yl)1-pentyl-1H-indazole-3-carboxamide
(ADB–PINACA), into schedule I of the
CSA (79 FR 7577), making all
regulations pertaining to schedule I
controlled substances applicable to the
manufacture of PB–22, 5F–PB–22, AB–
FUBINACA, and ADB–PINACA,
including the requirement to obtain a
manufacturing quota pursuant to 21
CFR part 1303.
The 2014 aggregate production quotas
for PB–22, 5F–PB–22, AB–FUBINACA,
and ADB–PINACA represent those
quantities that may be manufactured in
the United States in 2014 to provide for
the estimated scientific, research, and
industrial needs of the United States,
lawful export requirements, and the
establishment and maintenance of
reserve stocks.
On March 7, 2014, the DEA published
a notice titled, ‘‘Controlled Substances:
2014 Proposed Aggregate Production
Quota for Four Temporarily Controlled
Synthetic Cannabinoids’’ in the Federal
Register (79 FR 13076). That notice
proposed the 2014 aggregate production
quotas for PB–22, 5F–PB–22, AB–
VerDate Mar<15>2010
17:06 Apr 25, 2014
Jkt 232001
FUBINACA, and ADB–PINACA.
Interested persons were invited to
comment on or object to the proposed
aggregate production quotas for PB–22,
5F–PB–22, AB–FUBINACA, and ADB–
PINACA on or before April 7, 2014. No
comments were received.
Analysis for 2014 Established Aggregate
Production Quotas
In determining the 2014 aggregate
production quotas for quinolin-8-yl 1pentyl-1H-indole-3-carboxylate (PB–22),
quinolin-8-yl 1-(5-fluoropentyl)-1Hindole-3-carboxylate (5F–PB–22), N-(1amino-3-methyl-1-oxobutan-2-yl)-1-(4fluorobenzyl)-1H-indazole-3carboxamide (AB–FUBINACA), and N(1-amino-3,3-dimethyl-1-oxobutan-2-yl)1-pentyl-1H-indazole-3-carboxamide
(ADB–PINACA), the DEA has taken into
consideration the factors set forth at 21
CFR 1303.11, pursuant to 21 U.S.C.
826(a), and other relevant factors,
including 2014 export requirements,
industrial use, applications for quotas,
as well as information on research and
product development requirements.
Pursuant to 21 U.S.C. 826 and in
accordance with 21 CFR 1303.11, the
Deputy Administrator hereby
establishes the 2014 aggregate
production quotas for the PB–22, 5F–
PB–22, AB–FUBINACA, and ADB–
PINACA, expressed in grams of
anhydrous acid or base, as follows:
23377
DEPARTMENT OF LABOR
Office of the Secretary
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; Evaluating
the Accessibility of American Job
Centers for People With Disabilities
ACTION:
Notice.
The Department of Labor
(DOL) is submitting the information
collection request (ICR) proposal titled,
‘‘Evaluating the Accessibility of
American Job Centers for People with
Disabilities,’’ to the Office of
Management and Budget (OMB) for
review and approval for use in
accordance with the Paperwork
Reduction Act (PRA) of 1995 (44 U.S.C.
3501 et seq.). Public comments on the
ICR are invited.
SUMMARY:
The OMB will consider all
written comments that agency receives
on or before May 28, 2014.
DATES:
A copy of this ICR with
applicable supporting documentation;
including a description of the likely
respondents, proposed frequency of
response, and estimated total burden
may be obtained free of charge from the
RegInfo.gov Web site at https://
www.reginfo.gov/public/do/
PRAViewICR?ref_nbr=201403-1290-001
(this link will only become active on the
Established
Basic class—schedule I
day following publication of this notice)
2014 Quota
or by contacting Michel Smyth by
N-(1-amino-3,3-dimethyl-1telephone at 202–693–4129 (this is not
oxobutan-2-yl)-1-pentyla toll-free number) or by email at DOL_
1H-indazole-3PRA_PUBLIC@dol.gov.
carboxamide (ADB–
Submit comments about this request
PINACA) ............................
15 g
by mail or courier to the Office of
N-(1-amino-3-methyl-1Information and Regulatory Affairs,
oxobutan-2-yl)-1-(4fluorobenzyl)-1H-indazoleAttn: OMB Desk Officer for DOL–OS,
3-carboxamide (AB–
Office of Management and Budget,
FUBINACA) .......................
15 g Room 10235, 725 17th Street NW.,
quinolin-8-yl 1-(5Washington, DC 20503; by Fax: 202–
fluoropentyl)-1H-indole-3395–6881 (this is not a toll-free
carboxylate (5-fluoro-PB–
22; 5F–PB–22) ..................
15 g number); or by email: OIRA_
submission@omb.eop.gov. Commenters
quinolin-8-yl 1-pentyl-1Hare encouraged, but not required, to
indole-3-carboxylate (PB–
22; QUPIC) .......................
15 g send a courtesy copy of any comments
by mail or courier to the U.S.
In accordance with 21 CFR 1303.13,
Department of Labor—OASAM, Office
upon consideration of the relevant
of the Chief Information Officer, Attn:
factors, the Deputy Administrator may
Departmental Information Compliance
adjust the 2014 aggregate production
Management Program, Room N1301,
quotas for PB–22, 5F–PB–22, AB–
200 Constitution Avenue NW.,
FUBINACA, and ADB–PINACA as
Washington, DC 20210; or by email:
needed.
DOL_PRA_PUBLIC@dol.gov.
Dated: April 21, 2014.
Thomas M. Harrigan,
Deputy Administrator.
FOR FURTHER INFORMATION CONTACT:
[FR Doc. 2014–09556 Filed 4–25–14; 8:45 am]
Frm 00061
Fmt 4703
Michel Smyth by telephone at 202–693–
4129 (this is not a toll-free number) or
by email at DOL_PRA_PUBLIC@dol.gov.
Authority: 44 U.S.C. 3507(a)(1)(D).
BILLING CODE 4410–09–P
PO 00000
ADDRESSES:
Sfmt 4703
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Agencies
[Federal Register Volume 79, Number 81 (Monday, April 28, 2014)]
[Notices]
[Pages 23376-23377]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-09556]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-390]
Controlled Substances: 2014 Established Aggregate Production
Quotas for Four Temporarily Controlled Synthetic Cannabinoids
AGENCY: Drug Enforcement Administration (DEA), Department of Justice.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice establishes the initial 2014 aggregate production
quotas for four temporarily controlled synthetic cannabinoids: N-(1-
amino-3,3-dimethyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide
(ADB-PINACA); N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-
1H-indazole-3-carboxamide (AB-FUBINACA);
[[Page 23377]]
quinolin-8-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate (5-fluoro-PB-
22; 5F-PB-22); and quinolin-8-yl 1-pentyl-1H-indole-3-carboxylate (PB-
22; QUPIC).
DATES: Effective April 28, 2014.
FOR FURTHER INFORMATION CONTACT: Ruth A. Carter, Office of Diversion
Control, Drug Enforcement Administration; Mailing Address: 8701
Morrissette Drive, Springfield, Virginia 22152, Telephone: (202) 598-
6812.
SUPPLEMENTARY INFORMATION:
Background
Section 306 of the Controlled Substances Act (CSA) (21 U.S.C. 826)
requires the Attorney General to establish aggregate production quotas
for each basic class of controlled substance listed in schedules I and
II and for the list I chemicals ephedrine, pseudoephedrine, and
phenylpropanolamine. The Attorney General has delegated this authority
to the Administrator of the DEA, 28 CFR 0.100, who in turn has
redelegated that authority to the Deputy Administrator of the DEA, 28
CFR part 0, subpt. R, App.
On February 10, 2014, the DEA published in the Federal Register a
final order to temporarily place four synthetic cannabinoids, quinolin-
8-yl 1-pentyl-1H-indole-3-carboxylate (PB-22), quinolin-8-yl 1-(5-
fluoropentyl)-1H-indole-3-carboxylate (5F-PB-22), N-(1-amino-3-methyl-
1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide (AB-
FUBINACA), and N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-pentyl-1H-
indazole-3-carboxamide (ADB-PINACA), into schedule I of the CSA (79 FR
7577), making all regulations pertaining to schedule I controlled
substances applicable to the manufacture of PB-22, 5F-PB-22, AB-
FUBINACA, and ADB-PINACA, including the requirement to obtain a
manufacturing quota pursuant to 21 CFR part 1303.
The 2014 aggregate production quotas for PB-22, 5F-PB-22, AB-
FUBINACA, and ADB-PINACA represent those quantities that may be
manufactured in the United States in 2014 to provide for the estimated
scientific, research, and industrial needs of the United States, lawful
export requirements, and the establishment and maintenance of reserve
stocks.
On March 7, 2014, the DEA published a notice titled, ``Controlled
Substances: 2014 Proposed Aggregate Production Quota for Four
Temporarily Controlled Synthetic Cannabinoids'' in the Federal Register
(79 FR 13076). That notice proposed the 2014 aggregate production
quotas for PB-22, 5F-PB-22, AB-FUBINACA, and ADB-PINACA. Interested
persons were invited to comment on or object to the proposed aggregate
production quotas for PB-22, 5F-PB-22, AB-FUBINACA, and ADB-PINACA on
or before April 7, 2014. No comments were received.
Analysis for 2014 Established Aggregate Production Quotas
In determining the 2014 aggregate production quotas for quinolin-8-
yl 1-pentyl-1H-indole-3-carboxylate (PB-22), quinolin-8-yl 1-(5-
fluoropentyl)-1H-indole-3-carboxylate (5F-PB-22), N-(1-amino-3-methyl-
1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide (AB-
FUBINACA), and N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-pentyl-1H-
indazole-3-carboxamide (ADB-PINACA), the DEA has taken into
consideration the factors set forth at 21 CFR 1303.11, pursuant to 21
U.S.C. 826(a), and other relevant factors, including 2014 export
requirements, industrial use, applications for quotas, as well as
information on research and product development requirements.
Pursuant to 21 U.S.C. 826 and in accordance with 21 CFR 1303.11,
the Deputy Administrator hereby establishes the 2014 aggregate
production quotas for the PB-22, 5F-PB-22, AB-FUBINACA, and ADB-PINACA,
expressed in grams of anhydrous acid or base, as follows:
------------------------------------------------------------------------
Established
Basic class--schedule I 2014 Quota
------------------------------------------------------------------------
N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-pentyl-1H- 15 g
indazole-3-carboxamide (ADB-PINACA)....................
N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)- 15 g
1H-indazole-3-carboxamide (AB-FUBINACA)................
quinolin-8-yl 1-(5-fluoropentyl)-1H-indole-3-carboxylate 15 g
(5-fluoro-PB-22; 5F-PB-22).............................
quinolin-8-yl 1-pentyl-1H-indole-3-carboxylate (PB-22; 15 g
QUPIC).................................................
------------------------------------------------------------------------
In accordance with 21 CFR 1303.13, upon consideration of the
relevant factors, the Deputy Administrator may adjust the 2014
aggregate production quotas for PB-22, 5F-PB-22, AB-FUBINACA, and ADB-
PINACA as needed.
Dated: April 21, 2014.
Thomas M. Harrigan,
Deputy Administrator.
[FR Doc. 2014-09556 Filed 4-25-14; 8:45 am]
BILLING CODE 4410-09-P