Bulk Manufacturer of Controlled Substances Application: Promega Corporation, 33914 [2023-11175]

Download as PDF 33914 Federal Register / Vol. 88, No. 101 / Thursday, May 25, 2023 / Notices (Cannabis) as botanical raw material and/or active pharmaceutical ingredients (API) to DEA research registrants and manufacturers. No other activities for these drug codes are authorized for this registration. DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1202] Bulk Manufacturer of Controlled Substances Application: Royal Emerald Pharmaceuticals Matthew Strait, Deputy Assistant Administrator. Drug Enforcement Administration, Justice. ACTION: Notice of application. [FR Doc. 2023–11177 Filed 5–24–23; 8:45 am] Royal Emerald Pharmaceuticals 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 24, 2023. Such persons may also file a written request for a hearing on the application on or before July 24, 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 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 March 27, 2023, Royal Emerald Pharmaceuticals, 14011 Palm Drive, Building B, Desert Hot Springs, California 92240–6845, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): DEPARTMENT OF JUSTICE AGENCY: BILLING CODE P SUMMARY: lotter on DSK11XQN23PROD with NOTICES1 Controlled substance Marihuana Extract ........... Marihuana ........................ Tetrahydrocannabinols .... Drug code Schedule 7350 7360 7370 I I I The company plans to bulk manufacture the listed controlled substances to provide Marihuana VerDate Sep<11>2014 18:04 May 24, 2023 Jkt 259001 Drug Enforcement Administration Controlled substance Psilocybin ........................ Psilocyn ........................... Drug code Schedule 7437 7438 I I The company plans to bulk manufacture the listed controlled substances as Active Pharmaceutical Ingredients (API) for sale to its customers. No other activities for these drug codes are authorized for this registration. Matthew Strait, Deputy Assistant Administrator. [FR Doc. 2023–11175 Filed 5–24–23; 8:45 am] [Docket No. DEA–1200] BILLING CODE P Bulk Manufacturer of Controlled Substances Application: Promega Corporation Drug Enforcement Administration Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: [Docket No. DEA–1192] Promega Corporation 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 24, 2023. Such persons may also file a written request for a hearing on the application on or before July 24, 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 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 April 5, 2023, Promega Corporation, 3075 Sub Zero Parkway, Fitchburg, Wisconsin 53719, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUMMARY: PO 00000 Frm 00055 Fmt 4703 Sfmt 4703 DEPARTMENT OF JUSTICE Importer of Controlled Substances Application: Unither Manufacturing LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Unither Manufacturing LLC 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 June 26, 2023. Such persons may also file a written request for a hearing on the application on or before June 26, 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 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: SUMMARY: E:\FR\FM\25MYN1.SGM 25MYN1

Agencies

[Federal Register Volume 88, Number 101 (Thursday, May 25, 2023)]
[Notices]
[Page 33914]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-11175]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1200]


Bulk Manufacturer of Controlled Substances Application: Promega 
Corporation

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Promega Corporation 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 24, 2023. Such persons may also file a written request for a 
hearing on the application on or before July 24, 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 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 April 5, 2023, Promega Corporation, 3075 Sub Zero 
Parkway, Fitchburg, Wisconsin 53719, applied to be registered as a bulk 
manufacturer of the following basic class(es) of controlled 
substance(s):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Psilocybin..............................    7437  I
Psilocyn................................    7438  I
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances as Active Pharmaceutical Ingredients (API) for sale to its 
customers. No other activities for these drug codes are authorized for 
this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-11175 Filed 5-24-23; 8:45 am]
BILLING CODE P

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