Importer of Controlled Substances Application: SpecGX, LLC, 28153 [2021-10995]

Download as PDF Federal Register / Vol. 86, No. 99 / Tuesday, May 25, 2021 / Notices Controlled substance Thebaine ............................... Oxymorphone ....................... Phenazocine ......................... Carfentanil ............................. Fentanyl ................................ Drug code 9333 9652 9715 9743 9801 Schedule II II II II II The company plans to bulk manufacture the listed controlled substances for internal use 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. William T. McDermott, Assistant Administrator. [FR Doc. 2021–10996 Filed 5–24–21; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–838] Importer of Controlled Substances Application: SpecGX, LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: SpecGX, LLC. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before June 24, 2021. Such persons may also file a written request for a hearing on the application on or before June 24, 2021. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing should also 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. jbell on DSKJLSW7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 18:09 May 24, 2021 Jkt 253001 In accordance with 21 CFR 1301.34(a), this is notice that on February 5, 2021, SpecGX LLC, 3600 North 2nd Street, Saint Louis, Missouri 63147, applied to be registered as an importer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Controlled substance Marihuana ........................ Phenylacetone ................. Coca Leaves ................... Thebaine .......................... Opium, Raw ..................... Poppy Straw Concentrate Tapentadol ...................... Drug code Schedule 7360 8501 9040 9333 9600 9670 9780 I II II II II II II The company plans to import the listed controlled substances for bulk manufacture into Active Pharmaceutical Ingredients (API) for distribution to its customers. In reference to Tapentadol (9780) and Thebaine (9333), the company plans to import intermediate forms of these controlled substances for further manufacturing prior to distribution to its customers. In reference to drug code 7360 (Marihuana), the company plans to import synthetic cannabinol. No other activity for this drug is authorized for this registration. Placement of these codes onto the company’s registration does not translate into automatic approval of subsequent permit applications to import controlled substances. 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 the import of Food and Drug Administration-approved or nonapproved finished forms for commercial sale. William T. McDermott, Assistant Administrator. [FR Doc. 2021–10995 Filed 5–24–21; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE [OMB Number 1105–0008] Agency Information Collection Activities; Proposed eCollection eComments Requested; Extension of a Currently Approved Collection; Claim for Damage, Injury, or Death AGENCY: Civil Division, Department of Justice. ACTION: 60-Day notice. The Civil Division, Department of Justice (DOJ), will be SUMMARY: PO 00000 Frm 00101 Fmt 4703 Sfmt 4703 28153 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 July 26, 2021. FOR FURTHER INFORMATION CONTACT: Comments are encouraged and all comments should reference the 8 digit OMB number for the collection or the title of the collection. If you have questions concerning the collection, please contact James G. Touhey, Jr., Director, Torts Branch, Civil Division, U.S. Department of Justice, P.O. Box 888, Benjamin Franklin Station, Washington, DC 20044, Telephone: (202) 616–4400. Written comments and/or suggestions can also be directed to the Office of Management and Budget, Office of Information and Regulatory Affairs, Attention Department of Justice Desk Officer, Room 10235, 725 17th Street NW, Washington, DC 20503 or sent to OIRA_submissions@omb.eop.gov. 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 agency, 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; —Enhance the quality, utility, and clarity of the information to be collected; 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., permitting electronic submission of responses. Overview of This Information Collection 1. Type of Information Collection: Extension of a currently approved collection. 2. The Title of the Form/Collection: Claim for Damage, Injury, or Death. 3. The agency form number, if any, and the applicable component of the E:\FR\FM\25MYN1.SGM 25MYN1

Agencies

[Federal Register Volume 86, Number 99 (Tuesday, May 25, 2021)]
[Notices]
[Page 28153]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-10995]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-838]


Importer of Controlled Substances Application: SpecGX, LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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

SUMMARY: SpecGX, LLC. has applied to be registered as an importer of 
basic class(es) of controlled substance(s). Refer to Supplemental 
Information listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may file written comments on or objections to 
the issuance of the proposed registration on or before June 24, 2021. 
Such persons may also file a written request for a hearing on the 
application on or before June 24, 2021.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a 
hearing must be sent to: Drug Enforcement Administration, Attn: 
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All 
requests for a hearing should also 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.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on February 5, 2021, SpecGX LLC, 3600 North 2nd Street, 
Saint Louis, Missouri 63147, applied to be registered as an importer of 
the following basic class(es) of controlled substance(s):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Marihuana...............................    7360  I
Phenylacetone...........................    8501  II
Coca Leaves.............................    9040  II
Thebaine................................    9333  II
Opium, Raw..............................    9600  II
Poppy Straw Concentrate.................    9670  II
Tapentadol..............................    9780  II
------------------------------------------------------------------------

    The company plans to import the listed controlled substances for 
bulk manufacture into Active Pharmaceutical Ingredients (API) for 
distribution to its customers. In reference to Tapentadol (9780) and 
Thebaine (9333), the company plans to import intermediate forms of 
these controlled substances for further manufacturing prior to 
distribution to its customers. In reference to drug code 7360 
(Marihuana), the company plans to import synthetic cannabinol. No other 
activity for this drug is authorized for this registration. Placement 
of these codes onto the company's registration does not translate into 
automatic approval of subsequent permit applications to import 
controlled substances.
    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 the import of Food and Drug 
Administration-approved or non-approved finished forms for commercial 
sale.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2021-10995 Filed 5-24-21; 8:45 am]
BILLING CODE P
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