Certain Hydroxyprogesterone Caproate and Products Containing the Same; Notice of Receipt of Complaint; Solicitation of Comments Relating to the Public Interest, 65578-65579 [2012-26510]
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65578
Federal Register / Vol. 77, No. 209 / Monday, October 29, 2012 / Notices
Dated: September 26, 2012.
Lena McDowall,
Associate Director, Business Services.
[FR Doc. 2012–26466 Filed 10–26–12; 8:45 am]
BILLING CODE 4312–53–P
INTERNATIONAL TRADE
COMMISSION
[Docket No. 2919]
Certain Hydroxyprogesterone
Caproate and Products Containing the
Same; Notice of Receipt of Complaint;
Solicitation of Comments Relating to
the Public Interest
U.S. International Trade
Commission.
ACTION: Notice.
AGENCY:
Notice is hereby given that
the U.S. International Trade
Commission has received a complaint
entitled Certain Hydroxyprogesterone
Caproate and Products Containing the
Same, DN 2919; the Commission is
soliciting comments on any public
interest issues raised by the complaint
or complainant’s filing under section
210.8(b) of the Commission’s Rules of
Practice and Procedure (19 CFR
210.8(b)).
FOR FURTHER INFORMATION CONTACT: Lisa
R. Barton, Acting Secretary to the
Commission, U.S. International Trade
Commission, 500 E Street SW.,
Washington, DC 20436, telephone (202)
205–2000. The public version of the
complaint can be accessed on the
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov, and will be
available for inspection during official
business hours (8:45 a.m. to 5:15 p.m.)
in the Office of the Secretary, U.S.
International Trade Commission, 500 E
Street SW., Washington, DC 20436,
telephone (202) 205–2000.
General information concerning the
Commission may also be obtained by
accessing its Internet server (https://
www.usitc.gov). The public record for
this investigation may be viewed on the
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov. Hearingimpaired persons are advised that
information on this matter can be
obtained by contacting the
Commission’s TDD terminal on (202)
205–1810.
SUPPLEMENTARY INFORMATION: The
Commission has received a complaint
and a submission pursuant to section
210.8(b) of the Commission’s Rules of
Practice and Procedure filed on behalf
of K–V Pharmaceutical Company on
October 23, 2012. The complaint alleges
violations of section 337 of the Tariff
rmajette on DSK2TPTVN1PROD with
SUMMARY:
VerDate Mar<15>2010
13:18 Oct 26, 2012
Jkt 229001
Act of 1930 (19 U.S.C. 1337) in the
importation into the United States, the
sale for importation, and the sale within
the United States after importation of
certain hydroxyprogesterone caproate
and products containing the same. The
complaint names as respondents New
England Compounding Pharmacy, Inc.
of MA; Alwan Pharmacy &
Compounding Center of IL; Avella
Specialty Pharmacy of AZ; Bellevue
Pharmacy of MO; Betapharma
(Shanghai) Co., Ltd. of China;
Boudreaux’s Specialty Compounding of
LA; California Pharmacy &
Compounding Center of CA; College
Pharmacy of CO; Compound Care
Pharmacy of KY; Compounding
Solutions of AL; Daniel Drug of TX;
Five-Star Compounding Pharmacy of IA;
Fagron, Inc. of MN; Hawthorne
Pharmacy of SC; Health Dimensions
Compounding Pharmacy of MI;
Hopewell Pharmacy & Compounding
Center of NJ; Hubei Gedian Humanwell
Pharmaceutical Co., Ltd. of China;
Hubei Saibo Chemical Co., Ltd. of
China; Jinan Haohua Industry Co., Ltd.
of China; Kelley-Ross & Associates, Inc.
of WA; Lacey Drug Company/Marietta
Medical Center of GA; Letco Medical of
AL; Medisca, Inc. of NV; Owens
Healthcare Compounding Pharmacy of
CA; Partners In Care, Inc. of GA;
People’s Custom Rx of TN; Pharmerica
Corporation of KY; Prescription
Compounds of LA; Rye Beach Pharmacy
of NY; Sherry’s Drug Compounding and
Natural Pharmacy of OK; Shanghai
Jinhong Biopharmaceutical, Ltd. of
China; Stark Pharmacy of KS; The
Compounder Pharmacy of IL; The
Compounding Shoppe of AL; The
Medicine Shoppe Pharmacy of IL;
Triangle Compounding Pharmacy of NC;
Trinity Healthcare Medical Center of FL;
Universal Arts Pharmacy of FL; Village
Compounding of TX; Wedgewood
Pharmacy of NJ; Westmoreland
Pharmacy & Compounding of IN;
Williams Bros. Healthcare Pharmacy of
IN; Wilson Pharmacy, Inc. of TN;
Women’s International Pharmacy of WI;
Wuhan Xianghe Pharmaceutical, Co.,
Ltd. of China; and Xianju Hongyan
Pharmaceutical Chemicals Co., Ltd. of
China.
Proposed respondents, other
interested parties, and members of the
public are invited to file comments, not
to exceed five (5) pages in length,
inclusive of attachments, on any public
interest issues raised by the complaint
or section 210.8(b) filing. Comments
should address whether issuance of the
relief specifically requested by the
complainant in this investigation would
affect the public health and welfare in
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Fmt 4703
Sfmt 4703
the United States, competitive
conditions in the United States
economy, the production of like or
directly competitive articles in the
United States, or United States
consumers.
In particular, the Commission is
interested in comments that:
(i) Explain how the articles
potentially subject to the requested
remedial orders are used in the United
States;
(ii) Identify any public health, safety,
or welfare concerns in the United States
relating to the requested remedial
orders;
(iii) Identify like or directly
competitive articles that complainant,
its licensees, or third parties make in the
United States which could replace the
subject articles if they were to be
excluded;
(iv) Indicate whether complainant,
complainant’s licensees, and/or third
party suppliers have the capacity to
replace the volume of articles
potentially subject to the requested
exclusion order and/or a cease and
desist order within a commercially
reasonable time; and
(v) Explain how the requested
remedial orders would impact United
States consumers.
Written submissions must be filed no
later than by close of business, eight
calendar days after the date of
publication of this notice in the Federal
Register. There will be further
opportunities for comment on the
public interest after the issuance of any
final initial determination in this
investigation.
Persons filing written submissions
must file the original document
electronically on or before the deadlines
stated above and submit 8 true paper
copies to the Office of the Secretary by
noon the next day pursuant to section
210.4(f) of the Commission’s Rules of
Practice and Procedure (19 CFR
210.4(f)). Submissions should refer to
the docket number (‘‘Docket No. 2919’’)
in a prominent place on the cover page
and/or the first page. (See Handbook for
Electronic Filing Procedures, https://
www.usitc.gov/secretary/
fed_reg_notices/rules/
handbook_on_electronic_filing.pdf).
Persons with questions regarding filing
should contact the Secretary (202–205–
2000).
Any person desiring to submit a
document to the Commission in
confidence must request confidential
treatment. All such requests should be
directed to the Secretary to the
Commission and must include a full
statement of the reasons why the
Commission should grant such
E:\FR\FM\29OCN1.SGM
29OCN1
Federal Register / Vol. 77, No. 209 / Monday, October 29, 2012 / Notices
treatment. See 19 CFR 201.6. Documents
for which confidential treatment by the
Commission is properly sought will be
treated accordingly. All nonconfidential
written submissions will be available for
public inspection at the Office of the
Secretary and on EDIS.
This action is taken under the
authority of section 337 of the Tariff Act
of 1930, as amended (19 U.S.C. 1337),
and of sections 201.10 and 210.8(c) of
the Commission’s Rules of Practice and
Procedure (19 CFR 201.10, 210.8(c)).
By order of the Commission.
Issued: October 24, 2012.
Lisa R. Barton,
Acting Secretary to the Commission.
[FR Doc. 2012–26510 Filed 10–26–12; 8:45 am]
BILLING CODE 7020–02–P
INTERNATIONAL TRADE
COMMISSION
[Investigation No. 337–TA–805]
Certain Devices for Improving
Uniformity Used in a Backlight Module
and Components Thereof and
Products Containing Same; Notice of
Request for Statements on the Public
Interest
U.S. International Trade
Commission.
ACTION: Notice.
AGENCY:
Notice is hereby given that
the presiding administrative law judge
has issued a Final Initial Determination
and Recommended Determination on
Remedy and Bonding in the abovecaptioned investigation. The
Commission is soliciting comments on
public interest issues raised by the
recommended relief, specifically a
limited exclusion order against certain
devices for improving uniformity used
in a backlight module and components
thereof and products containing same
imported by respondents LG
Electronics, Inc. and LG Display Co.,
Ltd. both of Seoul, Republic of South
Korea (collectively ‘‘LG’’) and cease and
desist orders against LG.
FOR FURTHER INFORMATION CONTACT:
Megan M. Valentine, Office of the
General Counsel, U.S. International
Trade Commission, 500 E Street SW.,
Washington, DC 20436, telephone (202)
708–2301. The public version of the
complaint can be accessed on the
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov, and will be
available for inspection during official
business hours (8:45 a.m. to 5:15 p.m.)
in the Office of the Secretary, U.S.
rmajette on DSK2TPTVN1PROD with
SUMMARY:
VerDate Mar<15>2010
13:18 Oct 26, 2012
Jkt 229001
International Trade Commission, 500 E
Street SW., Washington, DC 20436,
telephone (202) 205–2000.
General information concerning the
Commission may also be obtained by
accessing its Internet server (https://
www.usitc.gov). The public record for
this investigation may be viewed on the
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov. Hearingimpaired persons are advised that
information on this matter can be
obtained by contacting the
Commission’s TDD terminal on (202)
205–1810.
SUPPLEMENTARY INFORMATION: Section
337 of the Tariff Act of 1930 provides
that if the Commission finds a violation
it shall exclude the articles concerned
from the United States:
Unless, after considering the effect of such
exclusion upon the public health and
welfare, competitive conditions in the United
States economy, the production of like or
directly competitive articles in the United
States, and United States consumers, it finds
that such articles should not be excluded
from entry.
19 U.S.C. 1337(d)(1). A similar
provision applies to cease and desist
orders. 19 U.S.C. 1337(f)(1).
The Commission is interested in
further development of the record on
the public interest in these
investigations. Accordingly, members of
the public are invited to file
submissions of no more than five (5)
pages, inclusive of attachments,
concerning the public interest in light of
the administrative law judge’s
Recommended Determination on
Remedy and Bonding issued in this
investigation on October 22, 2012.
Comments should address whether
issuance of a limited exclusion order
and cease and desist orders in this
investigation would affect the public
health and welfare in the United States,
competitive conditions in the United
States economy, the production of like
or directly competitive articles in the
United States, or United States
consumers.
In particular, the Commission is
interested in comments that:
(i) Explain how the articles
potentially subject to the recommended
orders are used in the United States;
(ii) Identify any public health, safety,
or welfare concerns in the United States
relating to the recommended orders;
(iii) Identify like or directly
competitive articles that complainant,
its licensees, or third parties make in the
United States which could replace the
subject articles if they were to be
excluded;
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Frm 00049
Fmt 4703
Sfmt 4703
65579
(iv) Indicate whether complainant,
complainant’s licensees, and/or third
party suppliers have the capacity to
replace the volume of articles
potentially subject to the recommended
exclusion order and/or a cease and
desist order within a commercially
reasonable time; and
(v) Explain how the limited exclusion
order and cease and desist orders would
impact consumers in the United States.
Written submissions must be filed no
later than by close of business on
November 21, 2012.
Persons filing written submissions
must file the original document
electronically on or before the deadlines
stated above and submit 8 true paper
copies to the Office of the Secretary by
noon the next day pursuant to section
210.4(f) of the Commission’s Rules of
Practice and Procedure (19 CFR
210.4(f)). Submissions should refer to
the investigation number (‘‘Inv. No.
337–TA–805’’) in a prominent place on
the cover page and/or the first page. (See
Handbook for Electronic Filing
Procedures, https://www.usitc.gov/
secretary/fed_reg_notices/rules/
handbook_on_electronic_filing.pdf).
Persons with questions regarding filing
should contact the Secretary (202–205–
2000).
Any person desiring to submit a
document to the Commission in
confidence must request confidential
treatment. All such requests should be
directed to the Secretary to the
Commission and must include a full
statement of the reasons why the
Commission should grant such
treatment. See 19 CFR 201.6. Documents
for which confidential treatment by the
Commission is properly sought will be
treated accordingly. A redacted nonconfidential version of the document
must also be filed simultaneously with
any confidential filing. All nonconfidential written submissions will be
available for public inspection at the
Office of the Secretary and on EDIS.
This action is taken under the
authority of section 337 of the Tariff Act
of 1930, as amended (19 U.S.C. 1337),
and of sections 201.10 and 210.50 of the
Commission’s Rules of Practice and
Procedure (19 CFR 201.10, 210.50).
Issued: October 24, 2012.
By order of the Commission.
Lisa R. Barton,
Acting Secretary to the Commission.
[FR Doc. 2012–26513 Filed 10–26–12; 8:45 am]
BILLING CODE 7020–02–P
E:\FR\FM\29OCN1.SGM
29OCN1
Agencies
[Federal Register Volume 77, Number 209 (Monday, October 29, 2012)]
[Notices]
[Pages 65578-65579]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-26510]
=======================================================================
-----------------------------------------------------------------------
INTERNATIONAL TRADE COMMISSION
[Docket No. 2919]
Certain Hydroxyprogesterone Caproate and Products Containing the
Same; Notice of Receipt of Complaint; Solicitation of Comments Relating
to the Public Interest
AGENCY: U.S. International Trade Commission.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the U.S. International Trade
Commission has received a complaint entitled Certain
Hydroxyprogesterone Caproate and Products Containing the Same, DN 2919;
the Commission is soliciting comments on any public interest issues
raised by the complaint or complainant's filing under section 210.8(b)
of the Commission's Rules of Practice and Procedure (19 CFR 210.8(b)).
FOR FURTHER INFORMATION CONTACT: Lisa R. Barton, Acting Secretary to
the Commission, U.S. International Trade Commission, 500 E Street SW.,
Washington, DC 20436, telephone (202) 205-2000. The public version of
the complaint can be accessed on the Commission's electronic docket
(EDIS) at https://edis.usitc.gov, and will be available for inspection
during official business hours (8:45 a.m. to 5:15 p.m.) in the Office
of the Secretary, U.S. International Trade Commission, 500 E Street
SW., Washington, DC 20436, telephone (202) 205-2000.
General information concerning the Commission may also be obtained
by accessing its Internet server (https://www.usitc.gov). The public
record for this investigation may be viewed on the Commission's
electronic docket (EDIS) at https://edis.usitc.gov. Hearing-impaired
persons are advised that information on this matter can be obtained by
contacting the Commission's TDD terminal on (202) 205-1810.
SUPPLEMENTARY INFORMATION: The Commission has received a complaint and
a submission pursuant to section 210.8(b) of the Commission's Rules of
Practice and Procedure filed on behalf of K-V Pharmaceutical Company on
October 23, 2012. The complaint alleges violations of section 337 of
the Tariff Act of 1930 (19 U.S.C. 1337) in the importation into the
United States, the sale for importation, and the sale within the United
States after importation of certain hydroxyprogesterone caproate and
products containing the same. The complaint names as respondents New
England Compounding Pharmacy, Inc. of MA; Alwan Pharmacy & Compounding
Center of IL; Avella Specialty Pharmacy of AZ; Bellevue Pharmacy of MO;
Betapharma (Shanghai) Co., Ltd. of China; Boudreaux's Specialty
Compounding of LA; California Pharmacy & Compounding Center of CA;
College Pharmacy of CO; Compound Care Pharmacy of KY; Compounding
Solutions of AL; Daniel Drug of TX; Five-Star Compounding Pharmacy of
IA; Fagron, Inc. of MN; Hawthorne Pharmacy of SC; Health Dimensions
Compounding Pharmacy of MI; Hopewell Pharmacy & Compounding Center of
NJ; Hubei Gedian Humanwell Pharmaceutical Co., Ltd. of China; Hubei
Saibo Chemical Co., Ltd. of China; Jinan Haohua Industry Co., Ltd. of
China; Kelley-Ross & Associates, Inc. of WA; Lacey Drug Company/
Marietta Medical Center of GA; Letco Medical of AL; Medisca, Inc. of
NV; Owens Healthcare Compounding Pharmacy of CA; Partners In Care, Inc.
of GA; People's Custom Rx of TN; Pharmerica Corporation of KY;
Prescription Compounds of LA; Rye Beach Pharmacy of NY; Sherry's Drug
Compounding and Natural Pharmacy of OK; Shanghai Jinhong
Biopharmaceutical, Ltd. of China; Stark Pharmacy of KS; The Compounder
Pharmacy of IL; The Compounding Shoppe of AL; The Medicine Shoppe
Pharmacy of IL; Triangle Compounding Pharmacy of NC; Trinity Healthcare
Medical Center of FL; Universal Arts Pharmacy of FL; Village
Compounding of TX; Wedgewood Pharmacy of NJ; Westmoreland Pharmacy &
Compounding of IN; Williams Bros. Healthcare Pharmacy of IN; Wilson
Pharmacy, Inc. of TN; Women's International Pharmacy of WI; Wuhan
Xianghe Pharmaceutical, Co., Ltd. of China; and Xianju Hongyan
Pharmaceutical Chemicals Co., Ltd. of China.
Proposed respondents, other interested parties, and members of the
public are invited to file comments, not to exceed five (5) pages in
length, inclusive of attachments, on any public interest issues raised
by the complaint or section 210.8(b) filing. Comments should address
whether issuance of the relief specifically requested by the
complainant in this investigation would affect the public health and
welfare in the United States, competitive conditions in the United
States economy, the production of like or directly competitive articles
in the United States, or United States consumers.
In particular, the Commission is interested in comments that:
(i) Explain how the articles potentially subject to the requested
remedial orders are used in the United States;
(ii) Identify any public health, safety, or welfare concerns in the
United States relating to the requested remedial orders;
(iii) Identify like or directly competitive articles that
complainant, its licensees, or third parties make in the United States
which could replace the subject articles if they were to be excluded;
(iv) Indicate whether complainant, complainant's licensees, and/or
third party suppliers have the capacity to replace the volume of
articles potentially subject to the requested exclusion order and/or a
cease and desist order within a commercially reasonable time; and
(v) Explain how the requested remedial orders would impact United
States consumers.
Written submissions must be filed no later than by close of
business, eight calendar days after the date of publication of this
notice in the Federal Register. There will be further opportunities for
comment on the public interest after the issuance of any final initial
determination in this investigation.
Persons filing written submissions must file the original document
electronically on or before the deadlines stated above and submit 8
true paper copies to the Office of the Secretary by noon the next day
pursuant to section 210.4(f) of the Commission's Rules of Practice and
Procedure (19 CFR 210.4(f)). Submissions should refer to the docket
number (``Docket No. 2919'') in a prominent place on the cover page
and/or the first page. (See Handbook for Electronic Filing Procedures,
https://www.usitc.gov/secretary/fed_reg_notices/rules/handbook_on_electronic_filing.pdf). Persons with questions regarding filing should
contact the Secretary (202-205-2000).
Any person desiring to submit a document to the Commission in
confidence must request confidential treatment. All such requests
should be directed to the Secretary to the Commission and must include
a full statement of the reasons why the Commission should grant such
[[Page 65579]]
treatment. See 19 CFR 201.6. Documents for which confidential treatment
by the Commission is properly sought will be treated accordingly. All
nonconfidential written submissions will be available for public
inspection at the Office of the Secretary and on EDIS.
This action is taken under the authority of section 337 of the
Tariff Act of 1930, as amended (19 U.S.C. 1337), and of sections 201.10
and 210.8(c) of the Commission's Rules of Practice and Procedure (19
CFR 201.10, 210.8(c)).
By order of the Commission.
Issued: October 24, 2012.
Lisa R. Barton,
Acting Secretary to the Commission.
[FR Doc. 2012-26510 Filed 10-26-12; 8:45 am]
BILLING CODE 7020-02-P