Notice2025-11249
Importer 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 18, 2025
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Veranova, L.P. 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 90 Issue 116 (Wednesday, June 18, 2025)</title>
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[Federal Register Volume 90, Number 116 (Wednesday, June 18, 2025)]
[Notices]
[Pages 26067-26068]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-11249]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1559]
Importer 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 an importer of
basic class(es) of controlled substance(s). Refer to Supplementary
Information listed below for further drug information.
[[Page 26068]]
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 18, 2025. Such persons may also file a written request for a
hearing on the application on or before July 18, 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. 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 May 5, 2025, Veranova, L.P., 2003 Nolte Drive, West
Deptford, New Jersey 08066-1727, 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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Coca Leaves..................... 9040 II
Thebaine........................ 9333 II
Opium, Raw...................... 9600 II
Noroxymorphone.................. 9668 II
Poppy Straw Concentrate......... 9670 II
Fentanyl........................ 9801 II
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The company plans to import Coca Leaves (9040), Opium, raw (9600),
and Poppy Straw Concentrate (9670) to bulk manufacture Active
Pharmaceutical Ingredients (API) for distribution to its customers. The
company plans to also import Thebaine (9333), Noroxymorphone (9668),
and Fentanyl (9801) to use as analytical reference standards, both
internally and to be sold to their customers to support testing of
Veranova, L.P. APIs only. 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. 2025-11249 Filed 6-17-25; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on June 18, 2025.
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