Notice2023-03410

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
February 17, 2023

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 88 Issue 33 (Friday, February 17, 2023)</title>
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[Federal Register Volume 88, Number 33 (Friday, February 17, 2023)]
[Notices]
[Pages 10381-10382]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-03410]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1148]


Bulk Manufacturer of Controlled Substances Application: Veranova, 
L.P.

AGENCY: Drug Enforcement Administration, Justice.

[[Page 10382]]


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 
April 18, 2023. Such persons may also file a written request for a 
hearing on the application on or before April 18, 2023.

ADDRESSES: The Drug Enforcement Administration (DEA) 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 January 5, 2023 Veranova, L.P., 25 Patton Road, 
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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                                           Drug
          Controlled substance             code          Schedule
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Amphetamine............................     1100  II
Methylphenidate........................     1724  II
Nabilone...............................     7379  II
Hydrocodone............................     9193  II
Levorphanol............................     9220  II
Thebaine...............................     9333  II
Alfentanil.............................     9737  II
Remifentanil...........................     9739  II
Sufentanil.............................     9740  II
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    The company plans to bulk manufacture the above controlled 
substances in order to support manufacturing and analytical testing 
activities at its other DEA-registered manufacturing facility. No other 
activities for these drug codes are authorized for this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-03410 Filed 2-16-23; 8:45 am]
BILLING CODE P


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Indexed from Federal Register on February 17, 2023.

This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.