Importer of Controlled Substances Application: Organic Standards Solutions International, LLC, 63101 [2022-22580]
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63101
Federal Register / Vol. 87, No. 200 / Tuesday, October 18, 2022 / Notices
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–1101]
Importer of Controlled Substances
Application: Organic Standards
Solutions International, LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Organic Standards Solutions
International, LLC 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
DATES:
the issuance of the proposed registration
on or before November 17, 2022. Such
persons may also file a written request
for a hearing on the application on or
before November 17, 2022.
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 September 20, 2022,
Organic Standards Solutions
International, LLC, 7290 Investment
Drive, Unit B, North Charleston, South
Carolina 29418–8305, applied to be
registered as an importer of the
following basic class(es) of controlled
substance(s):
Controlled substance
Drug code
Marihuana Extract ...........................................................................................................................................................
Marihuana ........................................................................................................................................................................
Tetrahydrocannabinols ....................................................................................................................................................
Psilocybin .........................................................................................................................................................................
Psilocyn ...........................................................................................................................................................................
The company plans to import the
listed controlled substances to produce
analytical reference standards for sale
and distribution to its customers. Drug
codes 7350 (Marihuana Extract) and
7360 (Marihuana) will be used for the
manufacture of cannabidiol only. In
reference to drug codes 7370
(Tetrahydrocannabinols) the company
plans to import a synthetic version of
this controlled substance. 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.
khammond on DSKJM1Z7X2PROD with NOTICES
Kristi O’Malley,
Assistant Administrator.
[FR Doc. 2022–22580 Filed 10–17–22; 8:45 am]
BILLING CODE P
VerDate Sep<11>2014
19:52 Oct 17, 2022
Jkt 259001
DEPARTMENT OF JUSTICE
[OMB Number 1125–0002]
Agency Information Collection
Activities; Proposed Collection
eComments Requested; Revision of a
Previously Approved Collection;
Notice of Appeal From a Decision of an
Immigration Judge
Executive Office for
Immigration Review, Department of
Justice.
ACTION: 30-Day notice.
AGENCY:
The Department of Justice
(DOJ), Executive Office for Immigration
Review, will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. This proposed
information collection was previously
published in the Federal Register at 87
FR 34905 (June 8, 2022), allowing for a
60-day comment period.
DATES: Comments are encouraged and
will be accepted for an additional 30
days until November 17, 2022.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments
especially on the estimated public
burden or associated response time,
SUMMARY:
PO 00000
Frm 00079
Fmt 4703
Sfmt 4703
7350
7360
7370
7437
7438
Schedule
I
I
I
I
I
suggestions, or need a copy of the
proposed information collection
instrument with instructions or
additional information, please contact
Lauren Alder Reid, Assistant Director,
Office of Policy, Executive Office for
Immigration Review, 5107 Leesburg
Pike, Suite 2500, Falls Church, VA
22041, telephone: (703) 305–0289.
Written comments and/or suggestions
can also be directed to the Office of
Management and Budget, Office of
Information and Regulatory Affairs,
Attention Department of Justice Desk
Officer, Washington, DC 20530 or sent
to OIRA_submissions@omb.eop.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;
E:\FR\FM\18OCN1.SGM
18OCN1
]]>Agencies
[Federal Register Volume 87, Number 200 (Tuesday, October 18, 2022)]
[Notices]
[Page 63101]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-22580]
[[Page 63101]]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1101]
Importer of Controlled Substances Application: Organic Standards
Solutions International, LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Organic Standards Solutions International, LLC 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
November 17, 2022. Such persons may also file a written request for a
hearing on the application on or before November 17, 2022.
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 September 20, 2022, Organic Standards Solutions
International, LLC, 7290 Investment Drive, Unit B, North Charleston,
South Carolina 29418-8305, applied to be registered as an importer of
the following basic class(es) of controlled substance(s):
------------------------------------------------------------------------
Controlled substance Drug code Schedule
------------------------------------------------------------------------
Marihuana Extract........................ 7350 I
Marihuana................................ 7360 I
Tetrahydrocannabinols.................... 7370 I
Psilocybin............................... 7437 I
Psilocyn................................. 7438 I
------------------------------------------------------------------------
The company plans to import the listed controlled substances to
produce analytical reference standards for sale and distribution to its
customers. Drug codes 7350 (Marihuana Extract) and 7360 (Marihuana)
will be used for the manufacture of cannabidiol only. In reference to
drug codes 7370 (Tetrahydrocannabinols) the company plans to import a
synthetic version of this controlled substance. 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.
Kristi O'Malley,
Assistant Administrator.
[FR Doc. 2022-22580 Filed 10-17-22; 8:45 am]
BILLING CODE P
