Importer of Controlled Substances Application: Wildlife Laboratories, Inc., 14914 [2017-05729]
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Federal Register / Vol. 82, No. 55 / Thursday, March 23, 2017 / Notices
Company
FR docket
Fisher Clinical Services, Inc ..........................................................................................................................
Sigma-Aldrich International:
GMBH-Sigma Aldrich Company LLC .....................................................................................................
Fisher Clinical Services, Inc ...................................................................................................................
Anderson Brecon, Inc ............................................................................................................................
Johnson Matthey Inc ..............................................................................................................................
Wildlife Laboratories, Inc ........................................................................................................................
Noramco, Inc ..........................................................................................................................................
Mylan Technologies, Inc ........................................................................................................................
81 FR 61248
September 6, 2016.
81
81
81
81
81
81
82
September 14, 2016.
October 4, 2016.
October 18, 2016.
October 18, 2016.
December 28, 2016.
December 28, 2016.
January 23, 2017.
The DEA has considered the factors in
21 U.S.C. 823, 952(a) and 958(a) and
determined that the registration of the
listed registrants to import the
applicable basic classes of schedule I or
II controlled substances is consistent
with the public interest and with United
States obligations under international
treaties, conventions, or protocols in
effect on May 1, 1971. The DEA
investigated each company’s
maintenance of effective controls
against diversion by inspecting and
testing each company’s physical
security systems, verifying each
company’s compliance with state and
local laws, and reviewing each
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 DEA has
granted a registration as an importer for
schedule I or II controlled substances to
the above listed persons.
Dated: March 17, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017–05730 Filed 3–22–17; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Application: Wildlife Laboratories, 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 1301.34(a) on
or before April 24, 2017. Such persons
may also file a written request for a
hearing on the application pursuant to
21 CFR 1301.43 on or before April 24,
2017.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DRW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for hearing must be
sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All requests for hearing
should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/LJ, 8701 Morrissette
DATES:
FR
FR
FR
FR
FR
FR
FR
63223
68455
71766
71766
95644
95640
7859
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DRW, 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, dispensers,
importers, and exporters of controlled
substances (other than final orders in
connection with suspension, denial, or
revocation of registration) has been
redelegated to the Assistant
Administrator of the DEA Diversion
Control Division (‘‘Assistant
Administrator’’) pursuant to section 7 of
28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR
1301.34(a), this is notice that on
February 2, 2017, Wildlife Laboratories,
Inc., 1230 W. Ash Street, Suite D,
Windsor, Colorado 80550–8055 applied
to be registered as an importer of the
following basic classes of controlled
substances:
SUPPLEMENTARY INFORMATION:
Controlled substance
Drug code
Etorphine (except HCl) ............................................................................................................................................
Etorphine HCl ..........................................................................................................................................................
Thiafentanil ..............................................................................................................................................................
sradovich on DSK3GMQ082PROD with NOTICES
The company plans to import the
listed controlled substances for sale to
its customers.
DEPARTMENT OF LABOR
Dated: March 17, 2017.
Louis J. Milione,
Assistant Administrator.
Agency Information Collection
Activities; Submission for OMB
Review; Comment Request; FederalState Unemployment Insurance
Program Data Exchange
Standardization
[FR Doc. 2017–05729 Filed 3–22–17; 8:45 am]
BILLING CODE 4410–09–P
Office of the Secretary
ACTION:
Notice.
18:27 Mar 22, 2017
Jkt 241001
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
Schedule
9056
9059
9729
I
II
II
and Training Administration (ETA)
sponsored information collection
request (ICR) titled, ‘‘Federal-State
Unemployment Insurance Program Data
Exchange Standardization,’’ 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). Public
comments on the ICR are invited.
The OMB will consider all
written comments that agency receives
on or before April 24, 2017.
DATES:
The Department of Labor
(DOL) is submitting the Employment
SUMMARY:
VerDate Sep<11>2014
Published
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]]>Agencies
[Federal Register Volume 82, Number 55 (Thursday, March 23, 2017)]
[Notices]
[Page 14914]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-05729]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Importer of Controlled Substances Application: Wildlife
Laboratories, Inc.
ACTION: Notice of application.
-----------------------------------------------------------------------
DATES: 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
1301.34(a) on or before April 24, 2017. Such persons may also file a
written request for a hearing on the application pursuant to 21 CFR
1301.43 on or before April 24, 2017.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/DRW,
8701 Morrissette Drive, Springfield, Virginia 22152. All requests for
hearing must be sent to: Drug Enforcement Administration, Attn:
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All
requests for hearing should also be sent to: (1) Drug Enforcement
Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette Drive,
Springfield, Virginia 22152; and (2) Drug Enforcement Administration,
Attn: DEA Federal Register Representative/DRW, 8701 Morrissette Drive,
Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: 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, dispensers, importers, and exporters of
controlled substances (other than final orders in connection with
suspension, denial, or revocation of registration) has been redelegated
to the Assistant Administrator of the DEA Diversion Control Division
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0,
appendix to subpart R.
In accordance with 21 CFR 1301.34(a), this is notice that on
February 2, 2017, Wildlife Laboratories, Inc., 1230 W. Ash Street,
Suite D, Windsor, Colorado 80550-8055 applied to be registered as an
importer of the following basic classes of controlled substances:
------------------------------------------------------------------------
Controlled substance Drug code Schedule
------------------------------------------------------------------------
Etorphine (except HCl).................. 9056 I
Etorphine HCl........................... 9059 II
Thiafentanil............................ 9729 II
------------------------------------------------------------------------
The company plans to import the listed controlled substances for
sale to its customers.
Dated: March 17, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017-05729 Filed 3-22-17; 8:45 am]
BILLING CODE 4410-09-P
