Bulk Manufacturer of Controlled Substances Application: Siegfried USA, LLC, 7173 [2025-01350]
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7173
Federal Register / Vol. 90, No. 12 / Tuesday, January 21, 2025 / Notices
substance(s). Refer to SUPPLEMENTARY
INFORMATION listed below for further
drug information.
DEPARTMENT OF JUSTICE
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 March 24, 2025. Such
persons may also file a written request
for a hearing on the application on or
before March 24, 2025.
[Docket No. DEA–1477]
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
https://www.regulations.gov 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 https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment.
ADDRESSES:
In
accordance with 21 CFR 1301.33(a), this
is notice that on September 27, 2024,
Groff Health Inc., 2218 South Queen
Street, York, Pennsylvania 17402–4631
applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Psilocybin .......................
Psilocyn ..........................
I
Drug
code
Schedule
7437
7438
I
I
I
The company plans to bulk
manufacture the listed controlled
substances for internal use or for sale to
its customers. No other activities for
these drug codes are authorized for this
registration.
ddrumheller on DSK120RN23PROD with NOTICES1
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025–01349 Filed 1–17–25; 8:45 am]
BILLING CODE P
VerDate Sep<11>2014
19:56 Jan 18, 2025
Jkt 265001
Drug
code
Schedule
9050
9143
9150
9193
9250
9254
9300
9330
9333
9630
9652
9780
II
II
II
II
II
II
II
II
II
II
II
II
Drug Enforcement Administration
DATES:
Controlled substance
Controlled substance
Bulk Manufacturer of Controlled
Substances Application: Siegfried
USA, LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Siegfried USA, LLC 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 March 24, 2025. Such
persons may also file a written request
for a hearing on the application on or
before March 24, 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
https://www.regulations.gov 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 https://www.regulations.gov. 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 November 20, 2024,
Siegfried USA, LLC, 33 Industrial Park
Road, Pennsville, New Jersey 08070–
3244 applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance(s):
SUMMARY:
Controlled substance
Gamma Hydroxybutyric
Acid.
Dihydromorphine ............
Hydromorphinol ..............
Amphetamine .................
Lisdexamfetamine ..........
Methylphenidate .............
Amobarbital ....................
Pentobarbital ..................
Secobarbital ....................
PO 00000
Frm 00103
Fmt 4703
Drug
code
Schedule
2010
I
9145
9301
1100
1205
1724
2125
2270
2315
I
I
II
II
II
II
II
II
Sfmt 4703
Codeine ..........................
Oxycodone .....................
Hydromorphone ..............
Hydrocodone ..................
Methadone ......................
Methadone intermediate
Morphine .........................
Oripavine ........................
Thebaine .........................
Opium tincture ................
Oxymorphone .................
Tapentadol ......................
The company plans to bulk
manufacture the listed controlled
substances in bulk for sale to its
customers. No other activities for these
drug codes are authorized for this
registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025–01350 Filed 1–17–25; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–1474]
Bulk Manufacturer of Controlled
Substances Application: Invizyne
Technologies, Inc.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Invizyne Technologies, Inc.
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 March 24, 2025. Such
persons may also file a written request
for a hearing on the application on or
before March 24, 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
https://www.regulations.gov 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
SUMMARY:
E:\FR\FM\21JAN1.SGM
21JAN1
Agencies
[Federal Register Volume 90, Number 12 (Tuesday, January 21, 2025)]
[Notices]
[Page 7173]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-01350]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1477]
Bulk Manufacturer of Controlled Substances Application: Siegfried
USA, LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Siegfried USA, LLC 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
March 24, 2025. Such persons may also file a written request for a
hearing on the application on or before March 24, 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 https://www.regulations.gov 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 https://www.regulations.gov. 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 November 20, 2024, Siegfried USA, LLC, 33 Industrial
Park Road, Pennsville, New Jersey 08070-3244 applied to be registered
as a bulk manufacturer of the following basic class(es) of controlled
substance(s):
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid.............. 2010 I
Dihydromorphine........................ 9145 I
Hydromorphinol......................... 9301 I
Amphetamine............................ 1100 II
Lisdexamfetamine....................... 1205 II
Methylphenidate........................ 1724 II
Amobarbital............................ 2125 II
Pentobarbital.......................... 2270 II
Secobarbital........................... 2315 II
Codeine................................ 9050 II
Oxycodone.............................. 9143 II
Hydromorphone.......................... 9150 II
Hydrocodone............................ 9193 II
Methadone.............................. 9250 II
Methadone intermediate................. 9254 II
Morphine............................... 9300 II
Oripavine.............................. 9330 II
Thebaine............................... 9333 II
Opium tincture......................... 9630 II
Oxymorphone............................ 9652 II
Tapentadol............................. 9780 II
------------------------------------------------------------------------
The company plans to bulk manufacture the listed controlled
substances in bulk for sale to its customers. No other activities for
these drug codes are authorized for this registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-01350 Filed 1-17-25; 8:45 am]
BILLING CODE P