Foreign-Trade Zone (FTZ) 22-Chicago, Illinois, Notification of Proposed Production Activity, AbbVie, Inc. (Pharmaceutical Products), North Chicago and Lake County, Illinois, 7989 [2021-02234]
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7989
Notices
Federal Register
Vol. 86, No. 21
Wednesday, February 3, 2021
This section of the FEDERAL REGISTER
contains documents other than rules or
proposed rules that are applicable to the
public. Notices of hearings and investigations,
committee meetings, agency decisions and
rulings, delegations of authority, filing of
petitions and applications and agency
statements of organization and functions are
examples of documents appearing in this
section.
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–04–2021]
jbell on DSKJLSW7X2PROD with NOTICES
Foreign-Trade Zone (FTZ) 22—
Chicago, Illinois, Notification of
Proposed Production Activity, AbbVie,
Inc. (Pharmaceutical Products), North
Chicago and Lake County, Illinois
AbbVie, Inc. (AbbVie) submitted a
notification of proposed production
activity to the FTZ Board for its
facilities in North Chicago and Lake
County, Illinois. The notification
conforming to the requirements of the
regulations of the FTZ Board (15 CFR
400.22) was received on January 27,
2021.
AbbVie already has authority to
produce pharmaceutical products
within Subzone 22S. The current
request would add a finished product
and a foreign status material to the
scope of authority. Pursuant to 15 CFR
400.14(b), additional FTZ authority
would be limited to the specific foreignstatus material and specific finished
product described in the submitted
notification (as described below) and
subsequently authorized by the FTZ
Board.
Production under FTZ procedures
could exempt AbbVie from customs
duty payments on the foreign-status
materials/components used in export
production. On its domestic sales, for
the foreign-status materials/components
noted below and in the existing scope
of authority, AbbVie would be able to
choose the duty rates during customs
entry procedures that applies to
IMBRUVICA® tablets (duty-free).
AbbVie would be able to avoid duty on
foreign-status components which
become scrap/waste. Customs duties
also could possibly be deferred or
reduced on foreign-status production
equipment.
The material sourced from abroad is
Ibrutinib active pharmaceutical
VerDate Sep<11>2014
17:21 Feb 02, 2021
Jkt 253001
ingredient (duty rate 6.5%). The request
indicates that Ibrutinib is subject to
duties under Section 301 of the Trade
Act of 1974 (Section 301), depending on
the country of origin. The applicable
Section 301 decisions require subject
merchandise to be admitted to FTZs in
privileged foreign status (19 CFR
146.41).
Public comment is invited from
interested parties. Submissions shall be
addressed to the Board’s Executive
Secretary and sent to: ftz@trade.gov. The
closing period for their receipt is March
15, 2021.
A copy of the notification will be
available for public inspection in the
‘‘Reading Room’’ section of the Board’s
website, which is accessible via
www.trade.gov/ftz.
For further information, contact
Christopher Wedderburn at
Chris.Wedderburn@trade.gov.
Dated: January 28, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021–02234 Filed 2–2–21; 8:45 am]
BILLING CODE 3510–DS–P
DEPARTMENT OF COMMERCE
International Trade Administration
[A–549–833]
Citric Acid and Certain Citrate Salts
From Thailand: Partial Rescission of
Antidumping Duty Administrative
Review, 2019–2020
Enforcement and Compliance,
International Trade Administration,
Department of Commerce.
SUMMARY: The Department of Commerce
(Commerce) is rescinding the
administrative review of the
antidumping duty order on citric acid
and certain citrate salts (citric acid) from
Thailand covering the period of review
(POR) July 1, 2019, through June 30,
2020, in part, with respect to Niran
(Thailand) Co., Ltd. (Niran), based on a
timely withdrawal of the request for
review for Niran.
DATES: Applicable February 3, 2021.
FOR FURTHER INFORMATION CONTACT: Joy
Zhang, AD/CVD Operations, Office III,
Enforcement and Compliance,
International Trade Administration,
U.S. Department of Commerce, 1401
Constitution Avenue NW, Washington,
DC 20230; telephone: (202) 482–1168.
AGENCY:
PO 00000
Frm 00001
Fmt 4703
Sfmt 4703
SUPPLEMENTARY INFORMATION:
Background
On July 1, 2020, Commerce published
in the Federal Register a notice of
opportunity to request an administrative
review of the antidumping duty order
on citric acid from Thailand for the
period July 1, 2019, through June 30,
2020.1 Based on timely requests from
COFCO Biochemical (Thailand) Co.,
Ltd. (COFCO), Sunshine Biotech
International Co., Ltd. (Sunshine), and
Archer Daniels Midland Company,
Cargill, Incorporated, and Tate & Lyle
Ingredients Americas LLC, domestic
producers of the subject merchandise
and petitioners in the original
investigation (collectively, the
petitioners),2 on September 3, 2020, in
accordance with 751(a)(1) of the Tariff
Act of 1930, as amended (the Act),
Commerce published in the Federal
Register a notice of initiation of
administrative review covering COFCO,
Sunshine, and Niran.3 On September
17, 2020, Commerce selected COFCO
and Sunshine for individual
examination and issued the
antidumping duty questionnaire to the
companies.4
On September 18, 2020, Niran filed a
no-shipment certification.5 On October
8, 2020, U.S. Customs and Border
Protection (CBP) confirmed that there
were no shipments of subject
merchandise from Niran during the
1 See Antidumping or Countervailing Duty Order,
Finding, or Suspended Investigation; Opportunity
to Request Administrative Review, 85 FR 39531
(July 1, 2020).
2 See COFCO’s Letter, ‘‘Citric Acid and Certain
Citrate Salts from Thailand: Request for
Administrative Review,’’ dated July 28, 2020; see
also Sunshine’s Letter, ‘‘Antidumping Duty
Investigation of Citric Acid and Certain Citrate Salts
from Thailand: Sunshine Biotech Request for
Review,’’ dated July 31, 2020; and Petitioners’
Letter, ‘‘Citric Acid and Certain Citrate Salts From
Thailand: Petitioners’ Request For Administrative
Review,’’ dated July 30, 2020 (the petitioners
requested review of COFCO, Sunshine, and Niran).
3 See Initiation of Antidumping and
Countervailing Duty Administrative Reviews, 85 FR
172 (September 3, 2020).
4 See Memorandum, ‘‘Antidumping Duty
Administrative Review of Citric Acid and Certain
Citrate Salts from Thailand; 2019–2020: Selection of
Respondents for Individual Examination,’’ dated
September 17, 2020. See also Antidumping
Questionnaires sent to COFCO and Sunshine, dated
September 21, 2020.
5 See Niran’s Letter, ‘‘Citric Acid and Certain
Citrate Salts from Thailand: No Shipment
Certification,’’ dated September 18, 2020.
E:\FR\FM\03FEN1.SGM
03FEN1
Agencies
[Federal Register Volume 86, Number 21 (Wednesday, February 3, 2021)]
[Notices]
[Page 7989]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-02234]
========================================================================
Notices
Federal Register
________________________________________________________________________
This section of the FEDERAL REGISTER contains documents other than rules
or proposed rules that are applicable to the public. Notices of hearings
and investigations, committee meetings, agency decisions and rulings,
delegations of authority, filing of petitions and applications and agency
statements of organization and functions are examples of documents
appearing in this section.
========================================================================
Federal Register / Vol. 86, No. 21 / Wednesday, February 3, 2021 /
Notices
[[Page 7989]]
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B-04-2021]
Foreign-Trade Zone (FTZ) 22--Chicago, Illinois, Notification of
Proposed Production Activity, AbbVie, Inc. (Pharmaceutical Products),
North Chicago and Lake County, Illinois
AbbVie, Inc. (AbbVie) submitted a notification of proposed
production activity to the FTZ Board for its facilities in North
Chicago and Lake County, Illinois. The notification conforming to the
requirements of the regulations of the FTZ Board (15 CFR 400.22) was
received on January 27, 2021.
AbbVie already has authority to produce pharmaceutical products
within Subzone 22S. The current request would add a finished product
and a foreign status material to the scope of authority. Pursuant to 15
CFR 400.14(b), additional FTZ authority would be limited to the
specific foreign-status material and specific finished product
described in the submitted notification (as described below) and
subsequently authorized by the FTZ Board.
Production under FTZ procedures could exempt AbbVie from customs
duty payments on the foreign-status materials/components used in export
production. On its domestic sales, for the foreign-status materials/
components noted below and in the existing scope of authority, AbbVie
would be able to choose the duty rates during customs entry procedures
that applies to IMBRUVICA[supreg] tablets (duty-free). AbbVie would be
able to avoid duty on foreign-status components which become scrap/
waste. Customs duties also could possibly be deferred or reduced on
foreign-status production equipment.
The material sourced from abroad is Ibrutinib active pharmaceutical
ingredient (duty rate 6.5%). The request indicates that Ibrutinib is
subject to duties under Section 301 of the Trade Act of 1974 (Section
301), depending on the country of origin. The applicable Section 301
decisions require subject merchandise to be admitted to FTZs in
privileged foreign status (19 CFR 146.41).
Public comment is invited from interested parties. Submissions
shall be addressed to the Board's Executive Secretary and sent to:
[email protected]. The closing period for their receipt is March 15, 2021.
A copy of the notification will be available for public inspection
in the ``Reading Room'' section of the Board's website, which is
accessible via www.trade.gov/ftz.
For further information, contact Christopher Wedderburn at
[email protected].
Dated: January 28, 2021.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2021-02234 Filed 2-2-21; 8:45 am]
BILLING CODE 3510-DS-P