Importer of Controlled Substances Application: Irvine Labs, Inc.

Primary source

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Published

June 29, 2023

Issuing agencies

Justice DepartmentDrug Enforcement Administration

Abstract

Irvine Labs, Inc. 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 88 Issue 124 (Thursday, June 29, 2023)</title>
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[Federal Register Volume 88, Number 124 (Thursday, June 29, 2023)]
[Notices]
[Page 42104]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-13812]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1197]


Importer of Controlled Substances Application: Irvine Labs, Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Irvine Labs, Inc. 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 31, 2023. Such persons may also file a written request for a 
hearing on the application on or before July 31, 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 <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 April 20, 2023, Irvine Labs, Inc. 7305 Murdy Circle, 
Huntington Beach, California 92647-3533, applied to be registered as an 
importer of the following basic class(es) of controlled substance(s).

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         Controlled substance           Drug code         Schedule
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Lysergic acid diethylamide...........        7315  I
Marihuana Extract....................        7350  I
Marihuana............................        7360  I
Tetrahydrocannabinols................        7370  I
Mescaline............................        7381  I
Peyote...............................        7415  I
Diethyltryptamine....................        7434  I
Dimethyltryptamine...................        7435  I
Psilocybin...........................        7437  I
Psilocyn.............................        7438  I
------------------------------------------------------------------------

    The company plans to import the bulk substances to support internal 
research, clinical trials, analytical purposes, and distribution to 
their customers. In reference to drug codes 7360 (Marihuana), 7350 
(Marihuana Extract), and 7370 (Tetrahydrocannabinols) the company plans 
to import a raw plant material and extracts. 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. 2023-13812 Filed 6-28-23; 8:45 am]
BILLING CODE P


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