Notice2023-19181
Importer of Controlled Substances Application: Lipomed
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
September 6, 2023
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Lipomed 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 88 Issue 171 (Wednesday, September 6, 2023)</title>
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[Federal Register Volume 88, Number 171 (Wednesday, September 6, 2023)]
[Notices]
[Pages 60988-60989]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-19181]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1257]
Importer of Controlled Substances Application: Lipomed
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Lipomed 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.
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
October 6, 2023. Such persons may also file a written request for a
hearing on the application on or before October 6, 2023.
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 July 28, 2023, Lipomed, 150 Cambridgepark Drive,
Suite 705, Cambridge, Massachusetts 02140-2300, 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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Etizolam (4-(2-chlorophenyl)-2-ethyl-9- 2780 I
methyl-6H-N thieno[3,2-
f][1,2,4]triazolo[4,3-a][1,4]diazepine.
Flualprazolam (8-chloro-6-(2- 2785 I
fluorophenyl)-1-methyl-4H-
benzo[f][1,2,4]triazolo[4,3-
a][1,4]diazepine).
Clonazolam (6-(2-chlorophenyl)-1-methyl-8- 2786 I
nitro-4H-benzo[f][1,2,4]triazolo[4,3-
a][1,4]diazepine.
Flubromazolam (8-bromo-6-(2-fluorophenyl)- 2788 I
1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-
a][1,4]diazepine.
[[Page 60989]]
Diclazepam (7-chloro-5-(2-chloro-5-(2- 2789 I
chlorophenyl)-1-methyl-1,3-dihydro-2H-
benzo[e][1,4]diazepin-2-one.
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The company plans to import the above listed controlled substances
as analytical reference standards for distribution to its customers for
research and analytics purposes. Placement of these drug codes onto the
company's registration does not translate into automatic approval of
subsequent permit applications to import controlled substances. 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.
Claude Redd,
Acting Deputy Assistant Administrator.
[FR Doc. 2023-19181 Filed 9-5-23; 8:45 am]
BILLING CODE P
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