Notice2025-21724
Bulk Manufacturer of Controlled Substances Application: Invizyne Technologies, 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
December 1, 2025
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Invizyne Technologies, 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 90 Issue 228 (Monday, December 1, 2025)</title>
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[Federal Register Volume 90, Number 228 (Monday, December 1, 2025)]
[Notices]
[Pages 55178-55179]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-21724]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1630]
Bulk Manufacturer of Controlled Substances Application: Invizyne
Technologies, Inc.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Invizyne Technologies, 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.
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 30, 2026. Such persons may also file a written request for a
hearing on the application on or before January 30, 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
[[Page 55179]]
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 October 29, 2025, Invizyne Technologies, Inc., 750
Royal Oaks Drive, Suite 106, Monrovia, California 91016-6357, applied
to be registered as a bulk manufacturer of the following basic
class(es) of controlled substance(s):
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Controlled substance Drug code Schedule
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Tetrahydrocannabinols................... 7370 I
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The company plans to bulk manufacture the listed controlled
substance for the internal use intermediates or for sale to its
customers. In reference to drug code 7370 (Tetrahydrocannabinols), the
company plans to bulk manufacture this drug as synthetic. No other
activity for this drug code is authorized for this registration.
Thomas Prevoznik,
Deputy Assistant Administrator.
[FR Doc. 2025-21724 Filed 11-28-25; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on December 1, 2025.
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