Bulk Manufacturer of Controlled Substances Application: Arista Biologicals, 41419 [2023-13466]

Download as PDF 41419 Federal Register / Vol. 88, No. 121 / Monday, June 26, 2023 / Notices The company plans to bulk manufacture the listed controlled substances for the internal use intermediates or for sale to its customers. The company plans to manufacture small quantities of the above-listed controlled substances as radiolabeled compounds for biochemical research. No other activities for these drug codes are authorized for this registration. ACTION: Notice of application. Arista Biologicals 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 August 25, 2023. Such persons may also file a written request for a hearing on the application on or before August 25, 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 SUMMARY: Matthew Strait, Deputy Assistant Administrator. [FR Doc. 2023–13473 Filed 6–23–23; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1203] Bulk Manufacturer of Controlled Substances Application: Arista Biologicals Drug Enforcement Administration, Justice. AGENCY: 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. In accordance with 21 CFR 1301.33(a), this is notice that on April 6, 2023, Arista Biologicals, 1101 Hamilton Street, Allentown, Pennsylvania 18101–1043, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Controlled substance Drug code 4-Anilino-N-Phenethyl-4-Piperidine (ANPP) ........................................................................................................................... Norfentanyl (N-phenyl-N-(piperidin-4-yl)propionamide) .......................................................................................................... The company plans to bulk manufacture the listed controlled substances for internal use as intermediates for formulation and analytical development purposes. No other activities for these drug codes are authorized for this registration. Matthew Strait, Deputy Assistant Administrator. [FR Doc. 2023–13466 Filed 6–23–23; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1220] Bulk Manufacturer of Controlled Substances Application: Olon Ricerca Bioscience LLC Drug Enforcement Administration, Justice. ddrumheller on DSK120RN23PROD with NOTICES1 AGENCY: ACTION: Notice of application. Olon Ricerca Bioscience 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 August 25, 2023. Such persons may also file a written request for a hearing on the application on or before August 25, 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 SUMMARY: In accordance with 21 CFR 1301.33(a), this is notice that on May 17, 2023, Olon Ricerca Bioscience LLC, 7528 Auburn Road, Concord Township, Ohio 44077– 9176 applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Amphetamine ................................................................................................................................................................................. Lisdexamfetamine .......................................................................................................................................................................... 19:33 Jun 23, 2023 Jkt 259001 PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 II II 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. Controlled substance VerDate Sep<11>2014 8333 8366 Schedule E:\FR\FM\26JNN1.SGM 26JNN1 Drug code Schedule 1100 1205 II II

Agencies

[Federal Register Volume 88, Number 121 (Monday, June 26, 2023)]
[Notices]
[Page 41419]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-13466]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1203]


Bulk Manufacturer of Controlled Substances Application: Arista 
Biologicals

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

-----------------------------------------------------------------------

SUMMARY: Arista Biologicals 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 
August 25, 2023. Such persons may also file a written request for a 
hearing on the application on or before August 25, 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 6, 2023, Arista Biologicals, 1101 Hamilton 
Street, Allentown, Pennsylvania 18101-1043, applied to be registered as 
a bulk manufacturer of the following basic class(es) of controlled 
substance(s):

------------------------------------------------------------------------
         Controlled substance            Drug code        Schedule
------------------------------------------------------------------------
4-Anilino-N-Phenethyl-4-Piperidine            8333  II
 (ANPP).
Norfentanyl (N-phenyl-N-(piperidin-4-         8366  II
 yl)propionamide).
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances for internal use as intermediates for formulation and 
analytical development purposes. No other activities for these drug 
codes are authorized for this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-13466 Filed 6-23-23; 8:45 am]
BILLING CODE P
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