Federal Register, Volume 86
Issue 21 (Wednesday, February 3, 2021)
[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]
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Notices
Federal Register
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This section of the FEDERAL
REGISTER contains documents other than rules
or proposed rules that are applicable to the public. Notices of
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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:
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]
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