Bulk Manufacturer of Controlled Substances Application: AUSTIN PHARMA, LLC, 34554 [2014-14144]
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34554
Federal Register / Vol. 79, No. 116 / Tuesday, June 17, 2014 / Notices
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Bulk Manufacturer of Controlled
Substances Application: AUSTIN
PHARMA, LLC
ACTION:
Notice of Correction.
In Federal Register document (FR
DOC) 2014–12944, on page 32322, in
the issue of Wednesday, June 4, 2014,
make the following correction:
On page 32322, in the second column,
the third paragraph, the first sentence
should read as follows:
In reference to drug code 7360, the
company plans to manufacture
synthetic cannabidiol in bulk for sale to
its customers.
Dated: June 10, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
the DEA Office of Diversion Control
(‘‘Deputy Assistant Administrator’’)
pursuant to sec. 7(g) of 28 CFR pt. 0,
subpt. R, App.
In accordance with 21 CFR
1301.33(a), this is notice that on
February 5, 2014, Euticals, Inc., 2460 W.
Bennett Street, Springfield, Missouri
65807–1229, applied to be registered as
a bulk manufacturer of the following
basic classes of controlled substances:
Controlled substance
Methadone (9250) ........................
Oripavine (9330) ...........................
Schedule
II
II
The company plans to manufacture
the listed controlled substances in bulk
for distribution and sale to its
customers.
Dated: June 10, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2014–14124 Filed 6–16–14; 8:45 am]
BILLING CODE 4410–09–P
[FR Doc. 2014–14144 Filed 6–16–14; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF LABOR
DEPARTMENT OF JUSTICE
[Docket No. DEA–392]
Bulk Manufacturer of Controlled
Substances Application: Euticals, Inc.
ACTION:
Notice of Application.
Registered bulk manufacturers of
the affected basic classes, and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration in
accordance with 21 CFR 1301.33(a) on
or before August 18, 2014.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/ODW, 8701
Morrissette Drive, Springfield, Virginia
22152.
The
Attorney General has delegated his
authority under the Controlled
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 redelegated to
the Deputy Assistant Administrator of
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VerDate Mar<15>2010
16:43 Jun 16, 2014
Jkt 232001
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; Records
of Tests and Examinations of Mine
Personnel Hoisting Equipment
ACTION:
DATES:
SUPPLEMENTARY INFORMATION:
Authority: 44 U.S.C. 3507(a)(1)(D).
Notice.
The Department of Labor
(DOL) is submitting the Mine Safety and
Health Administration (MSHA)
sponsored information collection
request (ICR) titled, ‘‘Records of Tests
and Examinations of Mine Personnel
Hoisting Equipment,’’ to the Office of
Management and Budget (OMB) for
review and approval for continued use,
without change, in accordance with the
Paperwork Reduction Act of 1995
(PRA), 44 U.S.C. 3501 et seq. Public
comments on the ICR are invited.
DATES: The OMB will consider all
written comments that agency receives
on or before July 17, 2014.
ADDRESSES: 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=201403-1219-003
(this link will only become active on the
day following publication of this notice)
or by contacting Michel Smyth by
telephone at 202–693–4129, TTY 202–
SUMMARY:
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
This ICR
seeks to extend PRA authority for the
Records of Tests and Examinations of
Mine Personnel Hoisting Equipment
information collection. Various MSHA
regulations make it mandatory for a
covered mine operator to make and
maintain records of specific tests and
inspections of mine personnel hoisting
systems, including wire ropes, to ensure
each system remains safe to operate
while in use. Mine Safety and Health
Act of 1977 section 103(h) authorizes
this information collection. See 30
U.S.C. 813(h).
This information collection is subject
to the PRA. A Federal agency generally
cannot conduct or sponsor a collection
of information, and the public is
generally not required to respond to an
information collection, unless it is
approved by the OMB under the PRA
and displays a currently valid OMB
Control Number. In addition,
notwithstanding any other provisions of
law, no person shall generally be subject
to penalty for failing to comply with a
collection of information that does not
display a valid Control Number. See 5
CFR 1320.5(a) and 1320.6. The DOL
obtains OMB approval for this
information collection under Control
Number 1219–0034.
OMB authorization for an ICR cannot
be for more than three (3) years without
renewal, and the current approval for
this collection is scheduled to expire on
July 31, 2014. The DOL seeks to extend
PRA authorization for this information
SUPPLEMENTARY INFORMATION:
Office of the Secretary
Drug Enforcement Administration
693–8064, (these are not toll-free
numbers) or by email at DOL_PRA_
PUBLIC@dol.gov.
Submit comments about this request
by mail or courier to the Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for DOL–
MSHA, Office of Management and
Budget, Room 10235, 725 17th Street
NW., Washington, DC 20503; by Fax:
202–395–6881 (this is not a toll-free
number); or by email: OIRA_
submission@omb.eop.gov. Commenters
are encouraged, but not required, to
send a courtesy copy of any comments
by mail or courier to the U.S.
Department of Labor-OASAM, Office of
the Chief Information Officer, Attn:
Departmental Information Compliance
Management Program, Room N1301,
200 Constitution Avenue NW.,
Washington, DC 20210; or by email:
DOL_PRA_PUBLIC@dol.gov.
FOR FURTHER INFORMATION CONTACT:
Contact Michel Smyth by telephone at
202–693–4129, TTY 202–693–8064,
(these are not toll-free numbers) or by
email at DOL_PRA_PUBLIC@dol.gov.
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]]>Agencies
[Federal Register Volume 79, Number 116 (Tuesday, June 17, 2014)]
[Notices]
[Page 34554]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-14144]
[[Page 34554]]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Bulk Manufacturer of Controlled Substances Application: AUSTIN
PHARMA, LLC
ACTION: Notice of Correction.
-----------------------------------------------------------------------
In Federal Register document (FR DOC) 2014-12944, on page 32322, in
the issue of Wednesday, June 4, 2014, make the following correction:
On page 32322, in the second column, the third paragraph, the first
sentence should read as follows:
In reference to drug code 7360, the company plans to manufacture
synthetic cannabidiol in bulk for sale to its customers.
Dated: June 10, 2014.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2014-14144 Filed 6-16-14; 8:45 am]
BILLING CODE 4410-09-P
