Bulk Manufacturer of Controlled Substances Application: Cargill, Inc., 16654-16655 [2020-06165]
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16654
Federal Register / Vol. 85, No. 57 / Tuesday, March 24, 2020 / Notices
The Siemon Company, Siemon Business
Park, 101 Siemon Company Drive,
Watertown, CT 06795.
Total Cable Solutions, Inc., 475 Victory
Drive, Springboro, OH 45066.
Wulei Technology Co., Ltd. d/b/a
Bonelinks, A409 Tangxi Jinggongfang,
Hongwan Commercial Center, Gushu,
Xixiang, Baoan District, Shenzhen,
China 518126.
lotter on DSKBCFDHB2PROD with NOTICES
(c) The Office of Unfair Import
Investigations, U.S. International Trade
Commission, 500 E Street SW, Suite
401, Washington, DC 20436; and
(4) For the investigation so instituted,
the Chief Administrative Law Judge,
U.S. International Trade Commission,
shall designate the presiding
Administrative Law Judge.
Responses to the complaint and the
notice of investigation must be
submitted by the named respondents in
accordance with section 210.13 of the
Commission’s Rules of Practice and
Procedure, 19 CFR 210.13. Pursuant to
19 CFR 201.16(e) and 210.13(a), such
responses will be considered by the
Commission if received not later than 20
days after the date of service by the
Commission of the complaint and the
notice of investigation. Extensions of
time for submitting responses to the
complaint and the notice of
investigation will not be granted unless
good cause therefor is shown.
Failure of a respondent to file a timely
response to each allegation in the
complaint and in this notice may be
deemed to constitute a waiver of the
right to appear and contest the
allegations of the complaint and this
notice, and to authorize the
administrative law judge and the
Commission, without further notice to
the respondent, to find the facts to be as
alleged in the complaint and this notice
and to enter an initial determination
and a final determination containing
such findings, and may result in the
issuance of an exclusion order or a cease
and desist order or both directed against
the respondent.
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–607]
Bulk Manufacturer of Controlled
Substances Application: Pisgah
Laboratories, Inc.
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before May 26, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.33(a), this
is notice that on February 3, 2020,
Pisgah Laboratories, Inc., 3222 Old
Hendersonville Highway, Pisgah Forest,
North Carolina 28768 applied to be
registered as a bulk manufacturer of the
following basic class(es) of controlled
substances:
DATES:
Drug
code
Controlled substance
Difenoxin .......................
Diphenoxylate ...............
Levorphanol ..................
Meperidine intermediate-B.
9168
9170
9220
9233
Schedule
I
II
II
II
The company plans to manufacture
the above-listed controlled substances
in bulk for distribution to its customers.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–06168 Filed 3–23–20; 8:45 am]
BILLING CODE 4410–09–P
hearing on the application on or before
April 23, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing must
be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All request for a hearing
should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on January 28, 2020, Sharp
(Bethlehem), LLC, 2400 Baglyos Circle,
Bethlehem, Pennsylvania 18020–8024
applied to be registered as an importer
of the following basic class(es) of
controlled substances:
Controlled substance
Gamma Hydroxybutyric
Acid.
3,4-Methylenedioxy
methamphetamine.
Psilocybin .....................
Drug
code
Schedule
2010
I
7405
I
7437
I
The company plans to import the
listed controlled substances for clinical
trials. Approval of permit applications
will occur only when the registrant’s
activity is consistent with what is
authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of FDA-approved or nonapproved finished dosage forms for
commercial sale.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–06167 Filed 3–23–20; 8:45 am]
DEPARTMENT OF JUSTICE
BILLING CODE 4410–09–P
Drug Enforcement Administration
[Docket No. DEA–605]
DEPARTMENT OF JUSTICE
By order of the Commission.
Issued: March 19, 2020.
Lisa Barton,
Secretary to the Commission.
Importer of Controlled Substances
Application: Sharp (Bethlehem), LLC
Drug Enforcement Administration
[FR Doc. 2020–06152 Filed 3–23–20; 8:45 am]
DATES:
ACTION:
BILLING CODE 7020–02–P
VerDate Sep<11>2014
17:34 Mar 23, 2020
Jkt 250001
Notice of application.
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before April 23, 2020. Such persons
may also file a written request for a
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[Docket No. DEA–608]
Bulk Manufacturer of Controlled
Substances Application: Cargill, Inc.
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
DATES:
E:\FR\FM\24MRN1.SGM
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Federal Register / Vol. 85, No. 57 / Tuesday, March 24, 2020 / Notices
issuance of the proposed registration on
or before May 26, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
In
accordance with 21 CFR 1301.33(a), this
is notice that on December 24, 2019,
Cargill, Inc., 17540 Monroe Wapello
Road, Eddyville, Iowa 52553 applied to
be registered as a bulk manufacturer of
the following basic class(es) of
controlled substance:
SUPPLEMENTARY INFORMATION:
Drug
code
Controlled substance
Gamma Hydroxybutyric
Acid.
2010
I
I
[FR Doc. 2020–06165 Filed 3–23–20; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–604]
Bulk Manufacturer of Controlled
Substances Application: Johnson
Matthey Inc.
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before May 26, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
DATES:
In
accordance with 21 CFR 1301.33(a), this
is notice that on February 7, 2020,
Johnson Matthey Inc., 2003 Nolte Drive,
West Deptford, New Jersey 08066–1742
applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance:
SUPPLEMENTARY INFORMATION:
lotter on DSKBCFDHB2PROD with NOTICES
4-Anilino-N-phenethyl-4piperidine (ANPP).
8333
II
I
I
The company plans to manufacture
the above-listed controlled substance
internally as intermediates or for sale to
their customers. No other activities for
this drug code is authorized for this
registration.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–06175 Filed 3–23–20; 8:45 am]
BILLING CODE 4410–09–P
Jkt 250001
Employment and Training
Administration
Notice of Determinations Regarding
Eligibility To Apply for Trade
Adjustment Assistance
In accordance with the Section 223
(19 U.S.C. 2273) of the Trade Act of
1974 (19 U.S.C. 2271, et seq.) (‘‘Act’’), as
amended, the Department of Labor
herein presents summaries of
determinations regarding eligibility to
apply for trade adjustment assistance
under Chapter 2 of the Act (‘‘TAA’’) for
workers by (TA–W) number issued
during the period of February 1, 2020
through February 29, 2020. (This Notice
primarily follows the language of the
Trade Act. In some places however,
changes such as the inclusion of
subheadings, a reorganization of
language, or ‘‘and,’’ ‘‘or,’’ or other words
are added for clarification.)
Section 222(a)—Workers of a Primary
Firm
Notice of application.
17:34 Mar 23, 2020
Schedule
DEPARTMENT OF LABOR
I
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
VerDate Sep<11>2014
Drug
code
Schedule
The company plans to manufacture
the above-listed controlled substance as
a byproduct. After analytical testing the
substance will be destroyed. No other
activities for this drug code is
authorized for this registration.
ACTION:
Controlled substance
In order for an affirmative
determination to be made for workers of
a primary firm and a certification issued
regarding eligibility to apply for TAA,
the group eligibility requirements under
Section 222(a) of the Act (19 U.S.C.
2272(a)) must be met, as follows:
(1) The first criterion (set forth in
Section 222(a)(1) of the Act, 19 U.S.C.
2272(a)(1)) is that a significant number
or proportion of the workers in such
workers’ firm (or ‘‘such firm’’) have
become totally or partially separated, or
are threatened to become totally or
partially separated;
16655
Shift in Production or Services to a
Foreign Country Path/Acquisition of
Articles or Services from a Foreign
Country Path, as follows:
(A) Increased Imports Path:
(i) The sales or production, or both, of
such firm, have decreased absolutely;
AND (ii and iii below)
(ii)(I) imports of articles or services
like or directly competitive with articles
produced or services supplied by such
firm have increased; OR
(II)(aa) imports of articles like or
directly competitive with articles into
which one or more component parts
produced by such firm are directly
incorporated, have increased; OR
(II)(bb) imports of articles like or
directly competitive with articles which
are produced directly using the services
supplied by such firm, have increased;
OR
(III) imports of articles directly
incorporating one or more component
parts produced outside the United
States that are like or directly
competitive with imports of articles
incorporating one or more component
parts produced by such firm have
increased;
AND
(iii) the increase in imports described
in clause (ii) contributed importantly to
such workers’ separation or threat of
separation and to the decline in the
sales or production of such firm; OR
(B) Shift in Production or Services to
a Foreign Country Path OR Acquisition
of Articles or Services from a Foreign
Country Path:
(i)(I) There has been a shift by such
workers’ firm to a foreign country in the
production of articles or the supply of
services like or directly competitive
with articles which are produced or
services which are supplied by such
firm; OR
(II) such workers’ firm has acquired
from a foreign country articles or
services that are like or directly
competitive with articles which are
produced or services which are
supplied by such firm;
AND
(ii) the shift described in clause (i)(I)
or the acquisition of articles or services
described in clause (i)(II) contributed
importantly to such workers’ separation
or threat of separation.
AND (2(A) or 2(B) below)
Section 222(b)—Adversely Affected
Secondary Workers
(2) The second criterion (set forth in
Section 222(a)(2) of the Act, 19 U.S.C.
2272(a)(2)) may be satisfied by either (A)
the Increased Imports Path, or (B) the
In order for an affirmative
determination to be made for adversely
affected secondary workers of a firm and
a certification issued regarding
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]]>Agencies
[Federal Register Volume 85, Number 57 (Tuesday, March 24, 2020)]
[Notices]
[Pages 16654-16655]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-06165]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-608]
Bulk Manufacturer of Controlled Substances Application: Cargill,
Inc.
ACTION: Notice of application.
-----------------------------------------------------------------------
DATES: Registered bulk manufacturers of the affected basic class(es),
and applicants therefore, may file written comments on or objections to
the
[[Page 16655]]
issuance of the proposed registration on or before May 26, 2020.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/DPW,
8701 Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this
is notice that on December 24, 2019, Cargill, Inc., 17540 Monroe
Wapello Road, Eddyville, Iowa 52553 applied to be registered as a bulk
manufacturer of the following basic class(es) of controlled substance:
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid.............. 2010 I
------------------------------------------------------------------------
The company plans to manufacture the above-listed controlled
substance as a byproduct. After analytical testing the substance will
be destroyed. No other activities for this drug code is authorized for
this registration.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-06165 Filed 3-23-20; 8:45 am]
BILLING CODE 4410-09-P
