Foreign-Trade Zone (FTZ) 93-Raleigh/Durham, North Carolina; Notification of Proposed Production Activity; GlaxoSmithKline, PLC (Pharmaceutical Products); Zebulon, North Carolina, 70531-70532 [2013-28353]
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Federal Register / Vol. 78, No. 228 / Tuesday, November 26, 2013 / Notices
Implementing Procedures (7 CFR part
372).
Done in Washington, DC, this 20th day of
November 2013.
Kevin Shea,
Administrator, Animal and Plant Health
Inspection Service.
[FR Doc. 2013–28322 Filed 11–25–13; 8:45 am]
BILLING CODE 3410–34–P
DEPARTMENT OF AGRICULTURE
Forest Service
Ashley Resource Advisory Committee
Forest Service, USDA.
Notice of meeting cancellation.
AGENCY:
ACTION:
The cancelled meeting was
to be held at the Ashley National Forest
Supervisor’s Office, Conference Room,
355 North Vernal Avenue, Vernal, Utah.
Written comments concerning this
cancellation may be submitted as
described under FOR FURTHER
INFORMATION CONTACT.
All comments, including names and
addresses when provided, are placed in
the record and are available for public
inspection and copying. The public may
inspect comments received at the
Ashley National Forest Supervisor’s
Office. Please call ahead to facilitate
entry into the building to view
comments.
FOR FURTHER INFORMATION CONTACT:
Louis Haynes, RAC Coordinator, by
phone at 435–781–5105 or email at:
lhaynes@fs.fed.us.
Individuals who use
telecommunication devices for the deaf
(TDD) may call the Federal Information
Relay Service (FIRS) at 1–800–877–8339
between 8:00 a.m. and 8:00 p.m.,
Eastern Standard Time, Monday
through Friday.
ADDRESSES:
The Ashley Resource
Advisory Committee (RAC) meeting
scheduled on the date below is
cancelled. The meeting was scheduled
to meet in Vernal, Utah. The RAC is
authorized under the Secure Rural
Schools and Community SelfDetermination Act (the Act) (Pub. L.
110–343) and operates in compliance
with the Federal Advisory Committee
Act (FACA) (Pub. L. 92–463).
DATES: The cancelled meeting was
scheduled for 6:00 p.m. on February 28,
2013.
SUMMARY:
Dated: November 5, 2013.
John R. Erickson,
Forest Supervisor.
[FR Doc. 2013–28189 Filed 11–25–13; 8:45 am]
70531
DEPARTMENT OF COMMERCE
Economic Development Administration
Notice of Petitions by Firms for
Determination of Eligibility To Apply
for Trade Adjustment Assistance
Economic Development
Administration, Department of
Commerce.
AGENCY:
Notice and opportunity for
public comment.
ACTION:
Pursuant to Section 251 of the Trade
Act 1974, as amended (19 U.S.C. 2341
et seq.), the Economic Development
Administration (EDA) has received
petitions for certification of eligibility to
apply for Trade Adjustment Assistance
from the firms listed below.
Accordingly, EDA has initiated
investigations to determine whether
increased imports into the United States
of articles like or directly competitive
with those produced by each of these
firms contributed importantly to the
total or partial separation of the firm’s
workers, or threat thereof, and to a
decrease in sales or production of each
petitioning firm.
BILLING CODE 3410–11–M
LIST OF PETITIONS RECEIVED BY EDA FOR CERTIFICATION ELIGIBILITY TO APPLY FOR TRADE ADJUSTMENT ASSISTANCE
[11/07/2013 through 11/20/2013]
Date accepted for
investigation
Firm name
Firm address
DryCase, LLC .........................................
349 Military Cutoff Road, Wilmington,
NC 28405.
1521 East McFadden Suite F, Santa
Ana, CA 92705.
emcdonald on DSK67QTVN1PROD with NOTICES
Benchmark Clothing
(dba—Benchmark
Benchmark FR).
Company,
Clothing
Inc.
and
Any party having a substantial
interest in these proceedings may
request a public hearing on the matter.
A written request for a hearing must be
submitted to the Trade Adjustment
Assistance for Firms Division, Room
71030, Economic Development
Administration, U.S. Department of
Commerce, Washington, DC 20230, no
later than ten (10) calendar days
following publication of this notice.
Please follow the requirements set
forth in EDA’s regulations at 13 CFR
315.9 for procedures to request a public
hearing. The Catalog of Federal
Domestic Assistance official number
and title for the program under which
these petitions are submitted is 11.313,
Trade Adjustment Assistance for Firms.
VerDate Mar<15>2010
18:04 Nov 25, 2013
Jkt 232001
11/08/2013
11/08/2013
Dated: November 20, 2013.
Michael DeVillo,
Eligibility Examiner.
[FR Doc. 2013–28302 Filed 11–25–13; 8:45 am]
BILLING CODE 3510–WH–P
DEPARTMENT OF COMMERCE
Foreign Trade Zones Board
[B–98–2013]
Foreign-Trade Zone (FTZ) 93—Raleigh/
Durham, North Carolina; Notification of
Proposed Production Activity;
GlaxoSmithKline, PLC (Pharmaceutical
Products); Zebulon, North Carolina
The Triangle J Council of
Governments, grantee of FTZ 93,
submitted a notification of proposed
PO 00000
Frm 00004
Fmt 4703
Sfmt 4703
Product(s)
The firm manufactures waterproof bags
for electronic devices.
The firm manufacturers flame resistant
garments.
production activity to the FTZ Board on
behalf of GlaxoSmithKline, PLC
(GlaxoSmithKline), located in Zebulon,
North Carolina. The notification
conforming to the requirements of the
regulations of the FTZ Board (15 CFR
400.22) was received on November 18,
2013.
The GlaxoSmithKline facility is
located within Site 6 of FTZ 93. The
facility is used for the production and
packaging of pharmaceutical products.
Pursuant to 15 CFR 400.14(b), FTZ
activity would be limited to the specific
foreign-status materials and components
and specific finished products listed in
the submitted notification (as described
below) and subsequently authorized by
the FTZ Board.
Production under FTZ procedures
could exempt GlaxoSmithKline from
E:\FR\FM\26NON1.SGM
26NON1
emcdonald on DSK67QTVN1PROD with NOTICES
70532
Federal Register / Vol. 78, No. 228 / Tuesday, November 26, 2013 / Notices
customs duty payments on the foreign
status components used in export
production. On its domestic sales,
GlaxoSmithKline would be able to
choose the duty rates during customs
entry procedures that apply to inhalers,
tablets, and capsules which treat a
variety of medical conditions (duty rates
range from free to 6.4%) for the foreign
status inputs noted below. Customs
duties also could possibly be deferred or
reduced on foreign status production
equipment.
The finished products include devices
such as respiratory placebo inhalers,
Relenza anti-viral inhalers, Seretide/
Advair, Serevent and Flovent diskus
respiratory inhalers, Advair and
Ventolin HFA respiratory inhalers, and
the following tablets and capules—
Lovaza antihyperlipidemic, Paxil
depression, Avandamet metabolic,
Avandary metabolic, Avandia
metabolic, Lamictal central nervous
system (CNS), Potiga CNS, Amerge CNS,
Horizant CNS, Imitrex CNS, Lamictal
ODT CNS, Requip/Requip XL CNS,
Treximet CNS, Telzir anti-viral, Valtrex
anti-viral, Zovirax anti-viral,
Wellbutrin/Buproprion depression,
Zantac gastrointestinal (GI), Zofran GI,
Votrient urology, Coreg CR
cardiovascular, Rythmol cardiovascular,
Innopran XL hypertension, Jalyn
urology, Avodart urology, Lanoxin
cardiovascular, Malarone anti-malarial,
Promacta immune thrombocytopenia
(ITP), and Tykerb oncology.
The components and materials
sourced from abroad include corn
starch, carnuba wax, lactose
monohydrate, fluticasone/salmeterol
placebo diskus (a type of inhaler),
respiratory placebo inhaler, silica
colloidal anhydrous, precipitated
calcium carbonate, pharmaceutical talc,
zephex 134a propellant, mannitol,
magnesium stearate, stearic acid,
potassium sorbate, propafenon hcl,
bupropion hydrochloride, melphalan,
albuterol sufate, salbuterol sulfate,
salmeterol, vilanterol trifenatate,
umeclidinium api, paracetamol,
ezogabine (retigabine), paracetamol,
metformin hydrochloride, ranitidine
hydrochloride, zanamivir, ondansetron
hydrochloride, abacavir sulfate,
valacyclovir hydrochloride, lamotrigine,
rosiglitazone maleate, paroxetine
hydrochloride, lamivudine, zidovudine,
pazopanib, fluticasone propionate,
fluticasone furoate, dutasteride, Lovaza
capsules, breo ellipta inhalers, avodart
capsules, flovent diskus, Paxil tablets,
lexiva oral suspension, sumatriptan
succinate/naproxen (Treximet),
abacavir/lamivudine tablets (epzicom)
tablets, atovaquone and proguanil hcl
tablets, combivir tablets, dolutegravir
VerDate Mar<15>2010
18:04 Nov 25, 2013
Jkt 232001
tablets, epivir tablets, epzicom tablets,
malarone tablets, ziagen tablets, Zantac
tablets, mekinist tablets, trametinib
tablets, pazopanib tablets, tafinlar
capsules, votrient tablets, coreg cr
capsules, flolan for injection,
propafenon sr, Rythmol (proafenon) sr,
Amerge tablets, imigran injection,
imitrex bulk pack, sumatriptan
succinate 85mg/naproxen, lamictal,
parnate tablets, ondansetron odt bulk,
requip tablets, soriatane (acitretin)
capsules, Zofran, Ventolin actuator dose
counter, Advair diskus, Advair diskus
inhalation powder, fluticasone/
salmeterol aerosol inhalers, Ventolin
samples, Seretide, argatroban, arixtra,
Avandamet tablets, Avandia tablets,
dutasteride-tamsulosin hcl fdc capsules,
eltrombopag, flolan sterile diluent, Jalyn
fixed dose combination capsules,
panadol tablets, opadry (an excipient),
starch pregel, Avandamet placebo
tablets, placebo diskus, nasal spray
demo pack, respiratory placebo,
triacetin, crospovidone, povidone,
spectracel, alginic acid ep, 20 micron
aluminum powder, empty aerosol cans,
pressure can spray valves, diskus
subassemblies, multi-dose powder
inhalers, novel dry powder inhalers,
multi-dose powder inhaler subassembly
and placebo, multi-dose powder inhaler
diskus devices, actuators—and their
dose counters and assemblies (duty
rates range from free to 6.5%).
Public comment is invited from
interested parties. Submissions shall be
addressed to the FTZ Board’s Executive
Secretary at the address below. The
closing period for their receipt is
January 6, 2014.
A copy of the notification will be
available for public inspection at the
Office of the Executive Secretary,
Foreign-Trade Zones Board, Room
21013, U.S. Department of Commerce,
1401 Constitution Avenue NW.,
Washington, DC 20230–0002, and in the
‘‘Reading Room’’ section of the FTZ
Board’s Web site, which is accessible
via www.trade.gov/ftz.
For further information, contact
Diane.Finver@trade.gov or (202) 482–
1367.
Dated: November 19, 2013.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2013–28353 Filed 11–25–13; 8:45 am]
BILLING CODE 3510–DS–P
PO 00000
Frm 00005
Fmt 4703
Sfmt 4703
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–99–2013]
Notification of Proposed Production
Activity, Hitachi Automotive Systems
Americas, Inc., Subzone 29F,
(Automotive Electric-Hybrid Drive
System Components), Harrodsburg,
Kentucky
The Louisville and Jefferson County
Riverport Authority, grantee of FTZ 29,
submitted a notification of proposed
production activity to the FTZ Board on
behalf of Hitachi Automotive Systems
Americas, Inc. (HIAMS–HK), operator of
Subzone 29F, at its facilities located in
Harrodsburg, Kentucky. The notification
conforming to the requirements of the
regulations of the FTZ Board (15 CFR
400.22) was received on November 12,
2013.
HIAMS–HK already has authority to
produce various automotive
components, including mass air sensors,
throttle bodies and chambers, starter
motors, motor/generator units,
alternators, distributors, other static
converters, inverter modules, rotors/
stators, batteries, ignition coils, sensors
and modules, fuel injectors, emissions
control equipment, valves, pumps, and
electronic control units for engines and
transmissions within Subzone 29F. The
current request would add finished
products (lithium-ion hybrid battery
pack assemblies, electrical power
steering modules, and electronic torque,
traction and transmission control
modules) and certain foreign
components to the scope of authority.
Pursuant to 15 CFR 400.14(b), FTZ
activity would be limited to the specific
foreign-status components and specific
finished products described in the
submitted notification (as described
below) and subsequently authorized by
the FTZ Board.
Production under FTZ procedures
could exempt HIAMS–HK from customs
duty payments on the foreign status
components used in export production.
On its domestic sales, HIAMS–HK
would be able to choose the duty rates
during customs entry procedures that
apply to lithium-ion hybrid battery pack
assemblies, rotors A&B, stators A&B,
electrical power steering modules, and
electronic torque, traction and
transmission control modules (free–
3.4%) for the foreign status inputs noted
below and in the existing scope of
authority. Customs duties also could
possibly be deferred or reduced on
foreign status production equipment.
The components and materials
sourced from abroad include: Plastic
E:\FR\FM\26NON1.SGM
26NON1
Agencies
[Federal Register Volume 78, Number 228 (Tuesday, November 26, 2013)]
[Notices]
[Pages 70531-70532]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-28353]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
Foreign Trade Zones Board
[B-98-2013]
Foreign-Trade Zone (FTZ) 93--Raleigh/Durham, North Carolina;
Notification of Proposed Production Activity; GlaxoSmithKline, PLC
(Pharmaceutical Products); Zebulon, North Carolina
The Triangle J Council of Governments, grantee of FTZ 93, submitted
a notification of proposed production activity to the FTZ Board on
behalf of GlaxoSmithKline, PLC (GlaxoSmithKline), located in Zebulon,
North Carolina. The notification conforming to the requirements of the
regulations of the FTZ Board (15 CFR 400.22) was received on November
18, 2013.
The GlaxoSmithKline facility is located within Site 6 of FTZ 93.
The facility is used for the production and packaging of pharmaceutical
products. Pursuant to 15 CFR 400.14(b), FTZ activity would be limited
to the specific foreign-status materials and components and specific
finished products listed in the submitted notification (as described
below) and subsequently authorized by the FTZ Board.
Production under FTZ procedures could exempt GlaxoSmithKline from
[[Page 70532]]
customs duty payments on the foreign status components used in export
production. On its domestic sales, GlaxoSmithKline would be able to
choose the duty rates during customs entry procedures that apply to
inhalers, tablets, and capsules which treat a variety of medical
conditions (duty rates range from free to 6.4%) for the foreign status
inputs noted below. Customs duties also could possibly be deferred or
reduced on foreign status production equipment.
The finished products include devices such as respiratory placebo
inhalers, Relenza anti-viral inhalers, Seretide/Advair, Serevent and
Flovent diskus respiratory inhalers, Advair and Ventolin HFA
respiratory inhalers, and the following tablets and capules--Lovaza
antihyperlipidemic, Paxil depression, Avandamet metabolic, Avandary
metabolic, Avandia metabolic, Lamictal central nervous system (CNS),
Potiga CNS, Amerge CNS, Horizant CNS, Imitrex CNS, Lamictal ODT CNS,
Requip/Requip XL CNS, Treximet CNS, Telzir anti-viral, Valtrex anti-
viral, Zovirax anti-viral, Wellbutrin/Buproprion depression, Zantac
gastrointestinal (GI), Zofran GI, Votrient urology, Coreg CR
cardiovascular, Rythmol cardiovascular, Innopran XL hypertension, Jalyn
urology, Avodart urology, Lanoxin cardiovascular, Malarone anti-
malarial, Promacta immune thrombocytopenia (ITP), and Tykerb oncology.
The components and materials sourced from abroad include corn
starch, carnuba wax, lactose monohydrate, fluticasone/salmeterol
placebo diskus (a type of inhaler), respiratory placebo inhaler, silica
colloidal anhydrous, precipitated calcium carbonate, pharmaceutical
talc, zephex 134a propellant, mannitol, magnesium stearate, stearic
acid, potassium sorbate, propafenon hcl, bupropion hydrochloride,
melphalan, albuterol sufate, salbuterol sulfate, salmeterol, vilanterol
trifenatate, umeclidinium api, paracetamol, ezogabine (retigabine),
paracetamol, metformin hydrochloride, ranitidine hydrochloride,
zanamivir, ondansetron hydrochloride, abacavir sulfate, valacyclovir
hydrochloride, lamotrigine, rosiglitazone maleate, paroxetine
hydrochloride, lamivudine, zidovudine, pazopanib, fluticasone
propionate, fluticasone furoate, dutasteride, Lovaza capsules, breo
ellipta inhalers, avodart capsules, flovent diskus, Paxil tablets,
lexiva oral suspension, sumatriptan succinate/naproxen (Treximet),
abacavir/lamivudine tablets (epzicom) tablets, atovaquone and proguanil
hcl tablets, combivir tablets, dolutegravir tablets, epivir tablets,
epzicom tablets, malarone tablets, ziagen tablets, Zantac tablets,
mekinist tablets, trametinib tablets, pazopanib tablets, tafinlar
capsules, votrient tablets, coreg cr capsules, flolan for injection,
propafenon sr, Rythmol (proafenon) sr, Amerge tablets, imigran
injection, imitrex bulk pack, sumatriptan succinate 85mg/naproxen,
lamictal, parnate tablets, ondansetron odt bulk, requip tablets,
soriatane (acitretin) capsules, Zofran, Ventolin actuator dose counter,
Advair diskus, Advair diskus inhalation powder, fluticasone/salmeterol
aerosol inhalers, Ventolin samples, Seretide, argatroban, arixtra,
Avandamet tablets, Avandia tablets, dutasteride-tamsulosin hcl fdc
capsules, eltrombopag, flolan sterile diluent, Jalyn fixed dose
combination capsules, panadol tablets, opadry (an excipient), starch
pregel, Avandamet placebo tablets, placebo diskus, nasal spray demo
pack, respiratory placebo, triacetin, crospovidone, povidone,
spectracel, alginic acid ep, 20 micron aluminum powder, empty aerosol
cans, pressure can spray valves, diskus subassemblies, multi-dose
powder inhalers, novel dry powder inhalers, multi-dose powder inhaler
subassembly and placebo, multi-dose powder inhaler diskus devices,
actuators--and their dose counters and assemblies (duty rates range
from free to 6.5%).
Public comment is invited from interested parties. Submissions
shall be addressed to the FTZ Board's Executive Secretary at the
address below. The closing period for their receipt is January 6, 2014.
A copy of the notification will be available for public inspection
at the Office of the Executive Secretary, Foreign-Trade Zones Board,
Room 21013, U.S. Department of Commerce, 1401 Constitution Avenue NW.,
Washington, DC 20230-0002, and in the ``Reading Room'' section of the
FTZ Board's Web site, which is accessible via www.trade.gov/ftz.
For further information, contact
Diane.Finver[com x mat]trade.gov or (202) 482-1367.
Dated: November 19, 2013.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2013-28353 Filed 11-25-13; 8:45 am]
BILLING CODE 3510-DS-P