Notice2026-18204
Bulk Manufacturer of Controlled Substances Application: Irvine Labs, Inc.
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
September 8, 2026
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Irvine Labs, Inc. has applied to be registered as a bulk manufacturer 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 91 Issue 172 (Tuesday, September 8, 2026)</title>
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[Federal Register Volume 91, Number 172 (Tuesday, September 8, 2026)]
[Notices]
[Pages 57165-57166]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-18204]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1765]
Bulk Manufacturer 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 a bulk
manufacturer
[[Page 57166]]
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 9, 2026. Such persons may also file a written request for a
hearing on the application on or before November 9, 2026.
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.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this
is notice that on August 13, 2026, Irvine Labs, Inc., 7305 Murdy
Circle, Huntington Beach, California 92647-3533, applied to be
registered as a bulk manufacturer 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
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The company plans to bulk manufacture bulk Active Pharmaceutical
Ingredients for product development and distribution to the Drug
Enforcement Administration-registered researchers. No other activities
for these drug codes are authorized for this registration.
Justin Wood,
Deputy Assistant Administrator.
[FR Doc. 2026-18204 Filed 9-4-26; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on September 8, 2026.
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