Importer of Controlled Substances Application: Veranova, L.P., 36335-36336 [2023-11740]
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lotter on DSK11XQN23PROD with NOTICES1
Federal Register / Vol. 88, No. 106 / Friday, June 2, 2023 / Notices
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 on the public
interest 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. Any
written submissions on other issues
must also be filed by no later than the
close of business, eight calendar days
after publication of this notice in the
Federal Register. Complainant may file
replies to any written submissions no
later than three calendar days after the
date on which any initial submissions
were due, notwithstanding § 201.14(a)
of the Commission’s Rules of Practice
and Procedure. No other submissions
will be accepted, unless requested by
the Commission. Any submissions and
replies filed in response to this Notice
are limited to five (5) pages in length,
inclusive of attachments.
Persons filing written submissions
must file the original document
electronically on or before the deadlines
stated above. Submissions should refer
to the docket number (‘‘Docket No.
3681’’) in a prominent place on the
cover page and/or the first page. (See
Handbook for Electronic Filing
Procedures, Electronic Filing
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17:34 Jun 01, 2023
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Procedures 1). Please note the
Secretary’s Office will accept only
electronic filings during this time.
Filings must be made through the
Commission’s Electronic Document
Information System (EDIS, https://
edis.usitc.gov.) No in-person paperbased filings or paper copies of any
electronic filings will be accepted until
further notice. Persons with questions
regarding filing should contact the
Secretary at EDIS3Help@usitc.gov.
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. All information,
including confidential business
information and documents for which
confidential treatment is properly
sought, submitted to the Commission for
purposes of this Investigation may be
disclosed to and used: (i) by the
Commission, its employees and Offices,
and contract personnel (a) for
developing or maintaining the records
of this or a related proceeding, or (b) in
internal investigations, audits, reviews,
and evaluations relating to the
programs, personnel, and operations of
the Commission including under 5
U.S.C. Appendix 3; or (ii) by U.S.
government employees and contract
personnel,2 solely for cybersecurity
purposes. All nonconfidential written
submissions will be available for public
inspection at the Office of the Secretary
and on EDIS.3
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 §§ 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: May 30, 2023.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2023–11774 Filed 6–1–23; 8:45 am]
BILLING CODE 7020–02–P
1 Handbook for Electronic Filing Procedures:
https://www.usitc.gov/documents/handbook_on_
filing_procedures.pdf.
2 All contract personnel will sign appropriate
nondisclosure agreements.
3 Electronic Document Information System
(EDIS): https://edis.usitc.gov.
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36335
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–1208]
Importer of Controlled Substances
Application: Veranova, L.P.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Veranova, L.P. has applied to
be registered as an importer of basic
class(es) of controlled substance(s).
Refer to SUPPLEMENTARY INFORMATION
listed below for further drug
information.
SUMMARY:
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before July 3, 2023. Such persons
may also file a written request for a
hearing on the application on or before
July 3, 2023.
ADDRESSES: The Drug Enforcement
Administration requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment. All
requests for a hearing must 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. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on April 19, 2023,
Veranova, L.P., 2003 Nolte Drive, West
Deptford, New Jersey 08066–1727,
applied to be registered as an importer
of the following basic class(es) of
controlled substance(s):
DATES:
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36336
Federal Register / Vol. 88, No. 106 / Friday, June 2, 2023 / Notices
Controlled substance
Coca Leaves ................
Thebaine .......................
Opium, raw ...................
Noroxymorphone ..........
Poppy Straw Concentrate.
Fentanyl ........................
Drug
code
Schedule
9040
9333
9600
9668
9670
II
II
II
II
II
9801
II
The company plans to import Coca
Leaves (9040), Opium, raw (9600), and
Poppy Straw Concentrate (9670) in
order to bulk manufacture Active
Pharmaceutical Ingredients (API) for
distribution to its customers. The
company plans to also import Thebaine
(9333), Noroxymorphone (9668), and
Fentanyl (9801) to use as analytical
reference standards, both internally and
to be sold to their customers to support
testing of Veranova, L.P. APIs only. No
other activities for these drug codes are
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.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023–11740 Filed 6–1–23; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
[OMB Number 1110–0046]
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Revision of a
Currently Approved Collection;
Friction Ridge Cards: Arrest and
Institution FD–249; Applicant FD–258;
Identity History Summary Request FD–
1164; FBI Standard Palm Print FD–884;
Supplemental Finger and Palm Print
FD–884a; Voluntary Appeal File
Fingerprint FD–1212; Firearm-Related
Challenge Fingerprint FD–1211
Federal Bureau of
Investigation, Criminal Justice
Information Services Division,
Department of Justice.
ACTION: 30-Day notice.
lotter on DSK11XQN23PROD with NOTICES1
AGENCY:
Department of Justice (DOJ),
Federal Bureau of Investigation (FBI),
Criminal Justice Information Services
(CJIS) Division will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
SUMMARY:
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17:34 Jun 01, 2023
Jkt 259001
accordance with the Paperwork
Reduction Act of 1995. The proposed
information collection was previously
published in the Federal Register,
Volume 88 pages 16664–16665, on
March 20, 2023, allowing a 60-day
comment period.
DATES: The DOJ encourages public
comment and will accept input until
July 3, 2023.
FOR FURTHER INFORMATION CONTACT: If
you have comments especially on the
estimated public burden or associated
response time, suggestions, or need a
copy of the proposed information
collection instrument with instructions
or additional information, please
contact: Larry E. Cotton-Zinn,
Management and Program Analyst, FBI,
CJIS, Criminal History Information and
Policy Unit, BTC–3, 1000 Custer Hollow
Road, Clarksburg, WV 26306; phone:
304–625–5590 or email fbi-iii@fbi.gov.
SUPPLEMENTARY INFORMATION: Written
comments and suggestions from the
public and affected agencies concerning
the proposed collection of information
are encouraged. Your comments should
address one or more of the following
four points:
—Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
—Evaluate the accuracy of the agency’s
estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
—Enhance the quality, utility, and
clarity of the information to be
collected; and/or
—Minimize the burden of the collection
of information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms
of information technology, e.g.,
permitting electronic submission of
responses.
Written comments and
recommendations for this information
collection should be submitted within
30 days of the publication of this notice
on the following website
www.reginfo.gov/public/do/PRAMain.
Find this particular information
collection by selecting ‘‘Currently under
30-day Review—Open for Public
Comments’’ or by using the search
function and entering either the title of
the information collection or the OMB
Control Number 1110–0046. This
information collection request may be
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Fmt 4703
Sfmt 4703
viewed at www.reginfo.gov. Follow the
instructions to view Department of
Justice, information collections
currently under review by OMB.
DOJ seeks PRA authorization for this
information collection for three (3)
years. OMB authorization for an ICR
cannot be for more than three (3) years
without renewal. The DOJ notes that
information collection requirements
submitted to the OMB for existing ICRs
receive a month-to-month extension
while they undergo review.
Overview of This Information
Collection
1. Type of Information Collection:
Revision of a currently approved
collection.
2. Title of the Form/Collection:
Friction Ridge Cards: Arrest and
Institution; Applicant; Identity History
Summary Request; FBI Standard Palm
Print; Supplemental Finger and Palm
Print; Voluntary Appeal File
Fingerprint; Firearm-Related Challenge
Fingerprint.
3. Agency form number, if any, and
the applicable component of the
Department sponsoring the collection:
Agency form number: Forms FD–249
(Arrest and Institution), FD–258
(Applicant), and FD–1164 (Identity
History Summary Request); FD–884 (FBI
Standard Palm Print); FD–884a
(Supplemental Finger and Palm Print);
FD–1212 (Voluntary Appeal File
Fingerprint); FD–1211 (Firearm-Related
Challenge Fingerprint) encompassed
under OMB 1110–0046; CJIS Division,
FBI, DOJ.
4. Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: City, county, state,
federal and tribal law enforcement
agencies; civil entities requesting
security clearance and background
checks. This collection is needed to
collect information on individuals
requesting background checks, security
clearance, or those individuals who
have been arrested for or accused of
criminal activities. Acceptable data is
stored as part of the Next Generation
Identification System (NGI) of the FBI.
5. Obligation to Respond: Required to
obtain or retain a benefit.
6. Total Estimated Number of
Respondents: 460,762.
7. Total Estimated Number of
Responses: 69,200,000.
8. Estimated Time per Respondent: 10
minutes.
9. Frequency: On occasion.
10. Total Estimated Annual Time
Burden: 11,500,000 hours.
11. Total Estimated Annual Other
Costs Burden: $0.
E:\FR\FM\02JNN1.SGM
02JNN1
]]>Agencies
[Federal Register Volume 88, Number 106 (Friday, June 2, 2023)]
[Notices]
[Pages 36335-36336]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-11740]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1208]
Importer of Controlled Substances Application: Veranova, L.P.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Veranova, L.P. has applied to be registered as an importer of
basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY
INFORMATION listed below for further drug information.
DATES: Registered bulk manufacturers of the affected basic class(es),
and applicants therefore, may submit electronic comments on or
objections to the issuance of the proposed registration on or before
July 3, 2023. Such persons may also file a written request for a
hearing on the application on or before July 3, 2023.
ADDRESSES: The Drug Enforcement Administration requires that all
comments be submitted electronically through the Federal eRulemaking
Portal, which provides the ability to type short comments directly into
the comment field on the web page or attach a file for lengthier
comments. Please go to https://www.regulations.gov and follow the
online instructions at that site for submitting comments. Upon
submission of your comment, you will receive a Comment Tracking Number.
Please be aware that submitted comments are not instantaneously
available for public view on https://www.regulations.gov. If you have
received a Comment Tracking Number, your comment has been successfully
submitted and there is no need to resubmit the same comment. All
requests for a hearing must 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. All requests for a hearing should also be
sent to: Drug Enforcement Administration, Attn: Administrator, 8701
Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this
is notice that on April 19, 2023, Veranova, L.P., 2003 Nolte Drive,
West Deptford, New Jersey 08066-1727, applied to be registered as an
importer of the following basic class(es) of controlled substance(s):
[[Page 36336]]
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Coca Leaves............................ 9040 II
Thebaine............................... 9333 II
Opium, raw............................. 9600 II
Noroxymorphone......................... 9668 II
Poppy Straw Concentrate................ 9670 II
Fentanyl............................... 9801 II
------------------------------------------------------------------------
The company plans to import Coca Leaves (9040), Opium, raw (9600),
and Poppy Straw Concentrate (9670) in order to bulk manufacture Active
Pharmaceutical Ingredients (API) for distribution to its customers. The
company plans to also import Thebaine (9333), Noroxymorphone (9668),
and Fentanyl (9801) to use as analytical reference standards, both
internally and to be sold to their customers to support testing of
Veranova, L.P. APIs only. No other activities for these drug codes are
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 non-approved finished
dosage forms for commercial sale.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-11740 Filed 6-1-23; 8:45 am]
BILLING CODE P
