Notice2025-09929
Bulk Manufacturer of Controlled Substances Application: Veranova, L.P.
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
June 2, 2025
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Veranova, L.P. 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 104 (Monday, June 2, 2025)</title>
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[Federal Register Volume 90, Number 104 (Monday, June 2, 2025)]
[Notices]
[Pages 23374-23375]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-09929]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1551]
Bulk Manufacturer of Controlled Substances Application: Veranova,
L.P.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Veranova, L.P. 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
August 1, 2025. Such persons may also file a written request for a
hearing on the application on or before August 1, 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.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this
is notice that on April 17, 2025, Veranova, L.P., 25 Patton Road,
Pharmaceutical Service, Devens, Massachusetts 01434-3803, 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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Lysergic Acid Diethylamide........ 7315 I
3,4-Methylenedioxymethamphetamine. 7405 I
Dimethyltryptamine................ 7435 I
Amphetamine....................... 1100 II
Methylphenidate................... 1724 II
Nabilone.......................... 7379 II
Hydrocodone....................... 9193 II
Levorphanol....................... 9220 II
Thebaine.......................... 9333 II
Alfentanil........................ 9737 II
[[Page 23375]]
Remifentanil...................... 9739 II
Sufentanil........................ 9740 II
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The company plans to bulk manufacture the listed controlled
substances in order to support the manufacturing and analytical testing
activities at its other Drug Enforcement Administration-registered
manufacturing facility. No other activities for these drug codes are
authorized for this registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-09929 Filed 5-30-25; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on June 2, 2025.
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