Notice2024-28717
Importer of Controlled Substances Application: Organic Standards Solutions International, LLC
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
December 6, 2024
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
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.
Full Text
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<title>Federal Register, Volume 89 Issue 235 (Friday, December 6, 2024)</title>
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[Federal Register Volume 89, Number 235 (Friday, December 6, 2024)]
[Notices]
[Pages 97070-97071]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2024-28717]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1465]
Importer of Controlled Substances Application: Organic Standards
Solutions International, LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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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
January 6, 2025. Such persons may also file a written request for a
hearing on the application on or before January 6, 2025.
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 <a href="https://www.regulations.gov">https://www.regulations.gov</a> 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 <a href="https://www.regulations.gov">https://www.regulations.gov</a>. 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 November 6, 2024, Organic Standards Solutions
International, LLC, 7290 Investment Drive, Unit B, North Charleston,
South
[[Page 97071]]
Carolina 29418-8305, applied to be registered as an importer of the
following basic class(es) of controlled substance(s):
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Drug
Controlled substance code Schedule
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Marihuana Extract....................... 7350 I
Marihuana............................... 7360 I
Tetrahydrocannabinols................... 7370 I
Psilocybin.............................. 7437 I
Psilocyn................................ 7438 I
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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 code 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.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2024-28717 Filed 12-5-24; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on December 6, 2024.
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