Bulk Manufacturer of Controlled Substances Application: Groff NA Hemplex LLC, 62117 [2022-22266]

Download as PDF 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]


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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.

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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
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