Importer of Controlled Substances Application: Fresenius Kabi USA, LLC, 79950-79951 [2024-22450]

Download as PDF 79950 Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices produced in each Subject Country, and such merchandise from other countries. (13) (OPTIONAL) A statement of whether you agree with the above definitions of the Domestic Like Product and Domestic Industry; if you disagree with either or both of these definitions, please explain why and provide alternative definitions. Authority: This proceeding is being conducted under authority of Title VII of the Tariff Act of 1930; this notice is published pursuant to § 207.61 of the Commission’s rules. By order of the Commission. Issued: September 25, 2024. Lisa Barton, Secretary to the Commission. [FR Doc. 2024–22441 Filed 9–30–24; 8:45 am] BILLING CODE 7020–02–P 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 22, 2024, Curia Wisconsin, Inc., 870 Badger Circle, Grafton, Wisconsin 53024–0000, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): ADDRESSES: DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1434] Bulk Manufacturer of Controlled Substances Application: Curia Wisconsin, Inc. Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Curia Wisconsin, 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 December 2, 2024. Such persons may also file a written request for a hearing on the application on or before December 2, 2024. SUMMARY: Controlled substance Drug code khammond on DSKJM1Z7X2PROD with NOTICES Lysergic acid diethylamide ..................................................................................................................................................... Tetrahydrocannabinols ........................................................................................................................................................... 4-Bromo-2,5-dimethoxyphenethylamine ................................................................................................................................. 3,4-Methylenedioxyamphetamine ........................................................................................................................................... 3,4-Methylenedioxymethamphetamine ................................................................................................................................... 5-Methoxy-N-N-dimethyltryptamine ........................................................................................................................................ Dimethyltryptamine ................................................................................................................................................................. Psilocybin ............................................................................................................................................................................... Psilocyn .................................................................................................................................................................................. Lisdexamfetamine .................................................................................................................................................................. Methylphenidate ..................................................................................................................................................................... Amobarbital ............................................................................................................................................................................ Nabilone ................................................................................................................................................................................. 4-Anilino-N-Phenethyl-4-Piperidine (ANPP) ........................................................................................................................... Opium extracts ....................................................................................................................................................................... Opium, powdered ................................................................................................................................................................... Opium, granulated .................................................................................................................................................................. Opium poppy .......................................................................................................................................................................... Noroxymorphone .................................................................................................................................................................... Fentanyl .................................................................................................................................................................................. The company plans to bulk manufacture the listed controlled substances for the purpose of analytical reference standards or for sale to its customers. In reference to the drug code 7370 (Tetrahydrocannabinols), the company plans to bulk manufacture as synthetic. No other activities for these drug codes are authorized for this registration. DEPARTMENT OF JUSTICE Marsha L. Ikner, Acting Deputy Assistant Administrator. ACTION: [FR Doc. 2024–22446 Filed 9–30–24; 8:45 am] BILLING CODE 4410–09–P VerDate Sep<11>2014 17:42 Sep 30, 2024 Jkt 265001 [Docket No. DEA–1435] Importer of Controlled Substances Application: Fresenius Kabi USA, LLC Drug Enforcement Administration, Justice. AGENCY: Notice of application. 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 October 31, 2024. Such persons may also file a written request for a hearing on the application on or before October 31, 2024. DATES: The Drug Enforcement Administration requires that all comments be submitted electronically through the Federal eRulemaking Portal, which provides the ability to type short ADDRESSES: Fresenius Kabi USA, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary PO 00000 Frm 00066 Fmt 4703 Sfmt 4703 I I I I I I I I I II II II II II II II II II II II Information listed below for further drug information. Drug Enforcement Administration SUMMARY: 7315 7370 7392 7400 7405 7431 7435 7437 7438 1205 1724 2125 7379 8333 9610 9639 9640 9650 9668 9801 Schedule E:\FR\FM\01OCN1.SGM 01OCN1 Federal Register / Vol. 89, No. 190 / Tuesday, October 1, 2024 / Notices 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 August 12, 2024, Fresenius Kabi USA, LLC, 3159 Staley Road, Grand Island, New York 14072– 2028, applied to be registered as an importer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Controlled substance Drug code Schedule Remifentanil .................. 9739 II khammond on DSKJM1Z7X2PROD with NOTICES The company plans to import the listed controlled substance(s) as bulk active pharmaceutical ingredient to manufacture Food and Drug Administration (FDA)-approved dosage forms. No other activity for this drug code is 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 FDA-approved or nonapproved finished dosage forms for commercial sale. Marsha L. Ikner, Acting Deputy Assistant Administrator. [FR Doc. 2024–22450 Filed 9–30–24; 8:45 am] BILLING CODE P VerDate Sep<11>2014 17:42 Sep 30, 2024 Jkt 265001 permitting electronic submission of responses. DEPARTMENT OF JUSTICE [OMB Number 1121–0329] Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension of a Previously Approved Collection; State Criminal Alien Assistance Program (SCAAP) Bureau of Justice Assistance, Department of Justice. ACTION: 60-Day notice. AGENCY: The Bureau of Justice Assistance, Department of Justice (DOJ), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. DATES: Comments are encouraged and will be accepted for 60 days until December 2, 2024. FOR FURTHER INFORMATION CONTACT: If you have additional comments especially on the estimated public burden or associated response time, suggestions, or need a copy of the proposed information collection instrument with instructions or additional information, please contact Joseph Husted, State Policy Advisor, Bureau of Justice Assistance, Department of Justice, 999 N Capitol St. NE, Washington, DC 20002; email: SCAAP@usdoj.gov; telephone: 202–598– 3617. SUPPLEMENTARY INFORMATION: Written comments and suggestions from the public and affected agencies concerning the proposed collection of information are encouraged. Your comments should address one or more of the following four points: —Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the Bureau of Justice Assistance, including whether the information will have practical utility; —Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; —Evaluate whether and if so how the quality, utility, and clarity of the information to be collected can be enhanced; and —Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., SUMMARY: PO 00000 Frm 00067 Fmt 4703 Sfmt 4703 79951 Abstract: In response to the Violent Crime Control and Law Enforcement Act of 1994, section 130002(b), as amended in 1996, BJA administers the State Criminal Alien Assistance Program (SCAAP) and the Department of Homeland Security (DHS). SCAAP provides federal payments to States and localities that incurred correctional officer salary costs for incarcerating undocumented criminal aliens with at least one felony or two misdemeanor convictions for violations of state or local law, and who are incarcerated for at least 4 consecutive days during the designated reporting period and for the following correctional purposes; Salaries for corrections officers Overtime costs Performance based bonuses Corrections work force recruitment and retention Construction of corrections facilities Training/education for offenders Training for corrections officers related to offender population management Consultants involved with offender population Medical and mental health services Vehicle rental/purchase for transport of offenders Prison Industries Pre-release/reentry programs Technology involving offender management/inter agency information sharing Disaster preparedness continuity of operations for corrections facilities Overview of This Information Collection 1. Type of Information Collection: Extension. 2. The Title of the Form/Collection: State Criminal Alien Assistance Program (SCAAP) (Authorizing Legislation: Section 241(i) of the Immigration and Nationality Act (8 U.S.C. 1231(i)). 3. The agency form number, if any, and the applicable component of the Department sponsoring the collection: The application process is managed through the internet, using the Office of Justice Programs’ (OJP) SCAAP online application system at: https:// bja.ojp.gov/program/state-criminalalien-assistance-program-scaap/ overview?Program_ID=86. 4. Affected public who will be asked or required to respond, as well as the obligation to respond: Affected Public: State, local and tribal governments. The obligation to respond is required to obtain/retain a benefit. E:\FR\FM\01OCN1.SGM 01OCN1

Agencies

[Federal Register Volume 89, Number 190 (Tuesday, October 1, 2024)]
[Notices]
[Pages 79950-79951]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-22450]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1435]


Importer of Controlled Substances Application: Fresenius Kabi 
USA, LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Fresenius Kabi USA, 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 
October 31, 2024. Such persons may also file a written request for a 
hearing on the application on or before October 31, 2024.

ADDRESSES: The Drug Enforcement Administration requires that all 
comments be submitted electronically through the Federal eRulemaking 
Portal, which provides the ability to type short

[[Page 79951]]

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.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on August 12, 2024, Fresenius Kabi USA, LLC, 3159 Staley 
Road, Grand Island, New York 14072-2028, applied to be registered as an 
importer of the following basic class(es) of controlled substance(s):

------------------------------------------------------------------------
                                          Drug
         Controlled substance             code           Schedule
------------------------------------------------------------------------
Remifentanil..........................     9739   II
------------------------------------------------------------------------

    The company plans to import the listed controlled substance(s) as 
bulk active pharmaceutical ingredient to manufacture Food and Drug 
Administration (FDA)-approved dosage forms. No other activity for this 
drug code is 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 FDA-approved or non-approved finished dosage forms for commercial 
sale.

Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-22450 Filed 9-30-24; 8:45 am]
BILLING CODE P
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