Notice2024-10084
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
May 9, 2024
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 89 Issue 91 (Thursday, May 9, 2024)</title>
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[Federal Register Volume 89, Number 91 (Thursday, May 9, 2024)]
[Notices]
[Page 39647]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2024-10084]
[[Page 39647]]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1367]
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
July 8, 2024. Such persons may also file a written request for a
hearing on the application on or before July 8, 2024.
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 8, 2024, Veranova, L.P., 2003 Nolte Drive, West
Deptford, New Jersey 08066-1727, 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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Gamma hydroxybutyric acid.................. 2010 I
Marihuana.................................. 7360 I
Tetrahydrocannabinols...................... 7370 I
3,4-Methylenedioxymethamphetamine.......... 7405 I
Psilocybin................................. 7437 I
Dihydromorphine............................ 9145 I
Difenoxin.................................. 9168 I
Fentanyl related-substances................ 9850 I
Amphetamine................................ 1100 II
Methamphetamine............................ 1105 II
Lisdexamfetamine........................... 1205 II
Methylphenidate............................ 1724 II
Nabilone................................... 7379 II
4-Anilino-N-Phenethyl-4-Piperidine (ANPP).. 8333 II
Norfentanyl (N-phenyl-N-(piperidin-4-yl) 8366 II
propionamide).
Cocaine.................................... 9041 II
Codeine.................................... 9050 II
Dihydrocodeine............................. 9120 II
Oxycodone.................................. 9143 II
Hydromorphone.............................. 9150 II
Diphenoxylate.............................. 9170 II
Ecgonine................................... 9180 II
Hydrocodone................................ 9193 II
Levorphanol................................ 9220 II
Meperidine................................. 9230 II
Methadone.................................. 9250 II
Methadone intermediate..................... 9254 II
Morphine................................... 9300 II
Thebaine................................... 9333 II
Opium tincture............................. 9630 II
Oxymorphone................................ 9652 II
Noroxymorphone............................. 9668 II
Alfentanil................................. 9737 II
Remifentanil............................... 9739 II
Sufentanil................................. 9740 II
Tapentadol................................. 9780 II
Fentanyl................................... 9801 II
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The company plans to bulk manufacture the listed controlled
substances for use as internal intermediates and for sale to its
customers. No other activities for these drug codes are authorized for
this registration.
Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-10084 Filed 5-8-24; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on May 9, 2024.
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