Bulk Manufacturer of Controlled Substances Application: Groff NA Hemplex LLC, 62117 [2022-22266]
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62117
Federal Register / Vol. 87, No. 197 / Thursday, October 13, 2022 / Notices
In accordance with 21 CFR
1301.33(a), DEA is providing notice that
on September 27, 2022, Irvine Labs,
Inc., 7305 Murdy Circle, Huntington
Beach, California 92647–3533, applied
to be registered as a bulk manufacturer
of the following basic class(es) of
controlled substances:
Drug
code
Controlled substance
Marihuana Extract ........
Marihuana .....................
Tetrahydrocannabinols
I
7350
7360
7370
Schedule
I
I
I
I
The applicant plans to manufacture
bulk APIs for product development and
distribution to DEA-registered
researchers. No other activities for these
drug codes are authorized for this
registration.
Kristi O’Malley,
Assistant Administrator.
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Bulk Manufacturer of Controlled
Substances Application: Groff NA
Hemplex LLC
khammond on DSKJM1Z7X2PROD with NOTICES
I
I
I
I
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Groff NA Hemplex 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 December 12, 2022. Such
persons may also file a written request
for a hearing on the application on or
before December 12, 2022.
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
[Docket No. DEA–1094]
Importer of Controlled Substances
Application: National Center for
Natural Products Research
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
National Center for Natural
Products Research 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.
SUMMARY:
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 November 14, 2022. Such
persons may also file a written request
for a hearing on the application on or
before November 14, 2022.
ADDRESSES: The Drug Enforcement
Administration requires that all
DATES:
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
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. 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.
In
accordance with 21 CFR 1301.34(a), this
is notice that on September 5, 2022,
National Center for Natural Products
Research, 806 Hathorn Road, 135 Coy
Waller Lab, University, Mississippi
38677, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
SUPPLEMENTARY INFORMATION:
BILLING CODE P
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
Jkt 259001
I
7350
7360
7370
[FR Doc. 2022–22266 Filed 10–12–22; 8:45 am]
AGENCY:
17:49 Oct 12, 2022
Marihuana Extract ........
Marihuana .....................
Tetrahydrocannabinols
Schedule
Kristi O’Malley,
Assistant Administrator.
[Docket No. DEA–1092]
VerDate Sep<11>2014
Drug
code
Controlled substance
The company is federally authorized
to conduct cultivation activities in order
to bulk manufacture the listed
controlled substances for internal use
and for sale to federally registered
research investigators. No other
activities for these drug codes are
authorized for this registration.
[FR Doc. 2022–22270 Filed 10–12–22; 8:45 am]
SUMMARY:
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 August 18, 2022, Groff
NA Hemplex LLC., 100 Redco Avenue,
Suite A, Red Lion, Pennsylvania 17356–
1436, applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance(s):
Drug
code
Controlled substance
Marihuana extract .........
Marihuana .....................
Tetrahydrocannabinols
I
7350
7360
7370
Schedule
I
I
I
I
The company plans to acquire new
genetic materials with improved
Cannabinoids for research and
manufacturing purposes. 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 nonapproved finished dosage forms for
commercial sale.
Kristi O’Malley,
Assistant Administrator.
[FR Doc. 2022–22267 Filed 10–12–22; 8:45 am]
BILLING CODE P
E:\FR\FM\13OCN1.SGM
13OCN1
Agencies
[Federal Register Volume 87, Number 197 (Thursday, October 13, 2022)]
[Notices]
[Page 62117]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-22266]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1092]
Bulk Manufacturer of Controlled Substances Application: Groff NA
Hemplex LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Groff NA Hemplex 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
December 12, 2022. Such persons may also file a written request for a
hearing on the application on or before December 12, 2022.
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 August 18, 2022, Groff NA Hemplex LLC., 100 Redco
Avenue, Suite A, Red Lion, Pennsylvania 17356-1436, applied to be
registered as a bulk manufacturer of the following basic class(es) of
controlled substance(s):
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Marihuana Extract...................... 7350 I
Marihuana.............................. 7360 I
Tetrahydrocannabinols.................. 7370 I
------------------------------------------------------------------------
The company is federally authorized to conduct cultivation
activities in order to bulk manufacture the listed controlled
substances for internal use and for sale to federally registered
research investigators. No other activities for these drug codes are
authorized for this registration.
Kristi O'Malley,
Assistant Administrator.
[FR Doc. 2022-22266 Filed 10-12-22; 8:45 am]
BILLING CODE P