Monosodium Glutamate From China and Indonesia, 68089-68090 [2020-23696]
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Federal Register / Vol. 85, No. 208 / Tuesday, October 27, 2020 / Notices
in the National Register of Historic
Places. Nominations for their
consideration were received by the
National Park Service before October 10,
2020. Pursuant to Section 60.13 of 36
CFR part 60, comments are being
accepted concerning the significance of
the nominated properties under the
National Register criteria for evaluation.
Before including your address, phone
number, email address, or other
personal identifying information in your
comment, you should be aware that
your entire comment—including your
personal identifying information—may
be made publicly available at any time.
While you can ask us in your comment
to withhold your personal identifying
information from public review, we
cannot guarantee that we will be able to
do so.
Nominations submitted by State or
Tribal Historic Preservation Officers:
ALABAMA
Mobile County
Midtown Historic District (Boundary
Increase), 2401–2403 and 2407 Old Shell
Rd., Mobile, BC100005805
Los Angeles County
Pasadena Field Archery Range, 415 South
Arroyo Blvd., Pasadena, SG100005799
Riverside County
Desert Golf Course, 301 North Belardo Rd.,
Palm Springs, SG100005813
San Francisco County
Whelan, John A., House, 1315 Waller St., San
Francisco, SG100005794
COLORADO
Denver County
First Avenue Hotel, 101 North Broadway,
Denver, SG100005800
Litchfield County
Winsted Water Works,Winchester Rd. (north
side), Old Waterbury Tpk./Rugg Brook Rd.,
Winchester, SG100005797
GEORGIA
Fulton County
Cascade Heights Commercial Historic
District, Centered on the jct. of Cascade Rd.
SW and Benjamin E. Hayes Dr. SW,
Atlanta, SG100005817
jbell on DSKJLSW7X2PROD with NOTICES
IOWA
MASSACHUSETTS
Suffolk County
Crawford Street Historic District, 5–38
Crawford St., 42 Elm Hill Ave., 621 Warren
St., Boston, SG100005798
Jkt 253001
Pima County
Armory Park Historic Residential District
(Additional Documentation), East 12th St.
to 19th St., Stone Ave. to 2nd Ave.,
Tucson, AD76000378
Hughes, Sam, Neighborhood Historic District
(Additional Documentation), Roughly
bounded by East Speedway Blvd., North
Campbell Ave., East 7th St. and North,
Bentley Ave., Tucson, AD94001164
OHIO
Stark County
St. Joseph Roman Catholic Church Complex,
2427 Tuscarawas St. West, Canton,
SG100005806
PUERTO RICO
KANSAS
San Juan Municipality
Rafael Cordero Graded School, (Early
Twentieth Century Schools in Puerto Rico
TR), Calle Aurora Esq. Horae Prada 15,
Santurce vicinity, MP100005816
Trego County
Wilcox School-District 29 & District 14
(Additional Documentation), (Public
Schools of Kansas MPS), Rural Route –15
mi. south of WaKeeney on KS 283,
Ransom, AD06000393
SOUTH DAKOTA
(Authority: Section 60.13 of 36 CFR part 60)
Roberts County
Sisseton School, (Schools in South Dakota
MPS), 302 East Maple St., Sisseton,
MP100005818
Sisseton School, (Federal Relief Construction
in South Dakota MPS), 302 East Maple St.,
Sisseton, MP100005818
Dated: October 14, 2020.
Sherry A. Frear,
Chief, National Register of Historic Places/
National Historic Landmarks Program.
[FR Doc. 2020–23681 Filed 10–26–20; 8:45 am]
BILLING CODE 4312–52–P
TENNESSEE
Montgomery County
Mt. Olive Cemetery, 951 Cumberland Dr.,
Clarksville, SG100005789
Rhea County
First Avenue Methodist Episcopal Church,
240 1st Ave., Dayton, SG100005790
Sullivan County
Kingsport Hosiery Mills, 435 Press St.,
Kingsport, SG100005791
Wayne County
Hughes House, 204 West Pillow St., Clifton,
SG100005793
VIRGINIA
Alexandria Independent City
George Washington High School, 1005 Mount
Vernon Ave., Alexandria, SG100005803
Craig County
Bellevue, 14505 Cumberland Gap Rd. (VA
42), New Castle vicinity, SG100005801
Halifax County
Oak Cliff, 10000 Huell Matthews Hwy. (US
501), Alton vicinity, SG100005804
Wapello County
Agassiz School, 608 East Williams St.,
Ottumwa, SG100005787
18:26 Oct 26, 2020
ARIZONA
Mercer County
V. Henry Rothschild-F.A. Straus and Co.
Atlantic Products Corporation Mill
Complex, 1 North Johnston Ave., Hamilton
Township, SG100005815
Washington County
Johnson City Postal Savings Bank and Post
Office, 401 Ashe St., Johnson City,
SG100005792
CONNECTICUT
VerDate Sep<11>2014
NEW JERSEY
Blount County
Millennium Manor, 500 North Wright Rd.,
Alcoa, SG100005788
CALIFORNIA
68089
Washington County
Depot Square Historic District, Wall St.
South, Depot Sq. SW, Front St. SW, Grand
St. SW, Abingdon, SG100005802
Additional documentation has been
received for the following resources:
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INTERNATIONAL TRADE
COMMISSION
[Investigation Nos. 731–TA–1229–1230
(Review)]
Monosodium Glutamate From China
and Indonesia
Determination
On the basis of the record 1 developed
in the subject five-year reviews, the
United States International Trade
Commission (‘‘Commission’’)
determines, pursuant to the Tariff Act of
1930 (‘‘the Act’’), that revocation of the
antidumping duty orders on
monosodium glutamate (‘‘MSG’’) from
China and Indonesia would be likely to
lead to continuation or recurrence of
material injury to an industry in the
United States within a reasonably
foreseeable time.
Background
The Commission instituted these
reviews on October 1, 2019 (84 FR
52129) and determined on January 6,
2020 that it would conduct full reviews
(85 FR 3421, January 21, 2020). Notice
of the scheduling of the Commission’s
reviews and of a public hearing to be
held in connection therewith was given
by posting copies of the notice in the
Office of the Secretary, U.S.
International Trade Commission,
Washington, DC, and by publishing the
1 The record is defined in § 207.2(f) of the
Commission’s Rules of Practice and Procedure (19
CFR 207.2(f)).
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68090
Federal Register / Vol. 85, No. 208 / Tuesday, October 27, 2020 / Notices
notice in the Federal Register on May
13, 2020 (85 FR 28663). In light of the
restrictions on access to the Commission
building due to the COVID–19
pandemic, the Commission conducted
its hearing through written testimony
and video conference on August 25,
2020. All persons who requested the
opportunity were permitted to
participate.
The Commission made these
determinations pursuant to section
751(c) of the Act (19 U.S.C. 1675(c)).
The Commission determined that these
reviews were extraordinarily
complicated and extended the review
period by up to 90 days. It completed
and filed its determinations in these
reviews on October 21, 2020. The views
of the Commission are contained in
USITC Publication 5127 (October 2020),
entitled Monosodium Glutamate from
China and Indonesia: Investigation Nos.
731–TA–1229–1230 (Review).
By order of the Commission.
Issued: October 21, 2020.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2020–23696 Filed 10–26–20; 8:45 am]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–736]
Importer of Controlled Substances
Application: Mylan Pharmaceuticals
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Mylan Pharmaceuticals has
applied to be registered as an importer
of basic class(es) of controlled
substance(s). Refer to Supplemental
Information listed below for further
drug information.
DATES: 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 November 27, 2020. Such
persons may also file a written request
for a hearing on the application on or
before November 27, 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,
jbell on DSKJLSW7X2PROD with NOTICES
VerDate Sep<11>2014
18:26 Oct 26, 2020
Jkt 253001
Controlled substance
Drug
code
Schedule
Amphetamine ...................
Methylphenidate ...............
Oxycodone .......................
Hydromorphone ................
Methadone ........................
Morphine ...........................
Fentanyl ............................
1100
1724
9143
9150
9250
9300
9801
II
II
II
II
II
II
II
The company plans to import finished
dosage forms for analytical testing and
distribution for clinical trials. No other
activity for these drug codes is
authorized for this registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
BILLING CODE 7020–02–P
SUMMARY:
Virginia 22152. All requests 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 October 7, 2020, Mylan
Pharmaceuticals, Incorporated, 3711
Collins Ferry Road, Morgantown, West
Virginia 26505–2362, applied to be
registered as an importer of the
following basic class(es) of controlled
substance(s):
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–23766 Filed 10–26–20; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–738]
Bulk Manufacturer of Controlled
Substances Application: Bulk
Manufacturer of Marihuana: API
GLOBAL LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
The Drug Enforcement
Administration (DEA) is providing
notice of an application it has received
from an entity applying to be registered
to manufacture in bulk basic class(es) of
SUMMARY:
PO 00000
Frm 00058
Fmt 4703
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controlled substances listed in schedule
I. DEA intends to evaluate this and other
pending applications according to
proposed regulations that, if finalized,
would govern the program of growing
marihuana for scientific and medical
research under DEA registration.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefor, may file written
comments on or objections to the
issuance of the proposed registration on
or before December 28, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW 8701
Morrissette Drive, Springfield, Virginia
22152. To ensure proper handling of
comments, please reference Docket No -.
DEA–738 in all correspondence,
including attachments.
SUPPLEMENTARY INFORMATION: The
Controlled Substances Act (CSA)
prohibits the cultivation and
distribution of marihuana except by
persons who are registered under the
CSA to do so for lawful purposes. In
accordance with the purposes specified
in 21 CFR 1301.33(a), DEA is providing
notice that the entity identified below
has applied for registration as a bulk
manufacturer of schedule I controlled
substances. In response, registered bulk
manufacturers of the affected basic
class(es), and applicants therefor, may
file written comments on or objections
of the requested registration, as
provided in this notice. This notice does
not constitute any evaluation or
determination of the merits of the
application submitted.
The applicant plans to manufacture
bulk active pharmaceutical ingredients
(APIs) for product development and
distribution to DEA registered
researchers. If the application for
registration is granted, the registrant
would not be authorized to conduct
other activity under this registration
aside from those coincident activities
specifically authorized by DEA
regulations. DEA will evaluate the
application for registration as a bulk
manufacturer for compliance with all
applicable laws, treaties, and
regulations and to ensure adequate
safeguards against diversion are in
place.
As this applicant has applied to
become registered as a bulk
manufacturer of marihuana, the
application will be evaluated under the
criteria of 21 U.S.C. 823(a). DEA
proposes to conduct this evaluation in
the manner described in the rule
proposed at 85 FR 16292, published on
March 23, 2020, if finalized.
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]]>Agencies
[Federal Register Volume 85, Number 208 (Tuesday, October 27, 2020)]
[Notices]
[Pages 68089-68090]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-23696]
=======================================================================
-----------------------------------------------------------------------
INTERNATIONAL TRADE COMMISSION
[Investigation Nos. 731-TA-1229-1230 (Review)]
Monosodium Glutamate From China and Indonesia
Determination
On the basis of the record \1\ developed in the subject five-year
reviews, the United States International Trade Commission
(``Commission'') determines, pursuant to the Tariff Act of 1930 (``the
Act''), that revocation of the antidumping duty orders on monosodium
glutamate (``MSG'') from China and Indonesia would be likely to lead to
continuation or recurrence of material injury to an industry in the
United States within a reasonably foreseeable time.
---------------------------------------------------------------------------
\1\ The record is defined in Sec. 207.2(f) of the Commission's
Rules of Practice and Procedure (19 CFR 207.2(f)).
---------------------------------------------------------------------------
Background
The Commission instituted these reviews on October 1, 2019 (84 FR
52129) and determined on January 6, 2020 that it would conduct full
reviews (85 FR 3421, January 21, 2020). Notice of the scheduling of the
Commission's reviews and of a public hearing to be held in connection
therewith was given by posting copies of the notice in the Office of
the Secretary, U.S. International Trade Commission, Washington, DC, and
by publishing the
[[Page 68090]]
notice in the Federal Register on May 13, 2020 (85 FR 28663). In light
of the restrictions on access to the Commission building due to the
COVID-19 pandemic, the Commission conducted its hearing through written
testimony and video conference on August 25, 2020. All persons who
requested the opportunity were permitted to participate.
The Commission made these determinations pursuant to section 751(c)
of the Act (19 U.S.C. 1675(c)). The Commission determined that these
reviews were extraordinarily complicated and extended the review period
by up to 90 days. It completed and filed its determinations in these
reviews on October 21, 2020. The views of the Commission are contained
in USITC Publication 5127 (October 2020), entitled Monosodium Glutamate
from China and Indonesia: Investigation Nos. 731-TA-1229-1230 (Review).
By order of the Commission.
Issued: October 21, 2020.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2020-23696 Filed 10-26-20; 8:45 am]
BILLING CODE 7020-02-P
