Bulk Manufacturer of Controlled Substances Application: Specgx, LLC, 51983-51984 [2018-22415]

Download as PDF 51983 Federal Register / Vol. 83, No. 199 / Monday, October 15, 2018 / Notices 42696, 42697 (2018). ‘‘Moreover, in the absence of an application (whether timely filed or not), there is nothing to act upon.’’ Reece, 77 FR at 35055, Rampey, 83 FR at 42697. Accordingly, because Registrant has allowed his registration to expire and has not filed an application to renew his registration or for any other registration in Alabama, this case is now moot and will be dismissed. Order Pursuant to 28 CFR 0.100(b) and the authority thus vested in me by 21 U.S.C. 824(a), I order that the Order to Show Cause issued to Phillip O. Rawlings, Jr., M.D., be, and it hereby is, dismissed. This Order is effective immediately. [FR Doc. 2018–22421 Filed 10–12–18; 8:45 am] BILLING CODE 4410–09–P The company listed below applied to be registered as an importer of various basic classes of controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted and no requests for hearing were submitted for these notices. SUPPLEMENTARY INFORMATION: DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Registration ACTION: registration by the Drug Enforcement Administration (DEA) as importers of various classes of schedule I or II controlled substances. Notice of registration. Registrant listed below have applied for and been granted SUMMARY: Company FR Docket Galephar Pharmaceutical Research Inc ................................. 83 FR 37525 .......................................................................... The Drug Enforcement Administration (DEA) has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of the listed registrant to import the applicable basic classes of schedule I or II controlled substances is consistent with the public interest and with United States obligations under international treaties, conventions, or protocols in effect on May 1, 1971. The DEA investigated the company’s maintenance of effective controls against diversion by inspecting and testing each company’s physical security systems, verifying the company’s compliance with state and local laws, and reviewing the company’s background and history. Therefore, pursuant to 21 U.S.C. 952(a) and 958(a), and in accordance with 21 CFR 1301.34, the DEA has granted a registration as an importer for schedule I or II controlled substance to the above listed company. Dated: September 24, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2018–22420 Filed 10–12–18; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE khammond on DSK30JT082PROD with NOTICES Dated: September 26, 2018. Uttam Dhillon, Acting Administrator. Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Application: Cambrex High Point, Inc. ACTION: Notice of application. VerDate Sep<11>2014 21:34 Oct 12, 2018 Jkt 247001 Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before November 14, 2018. Such persons may also file a written request for a hearing on the application on or before November 14, 2018. 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 hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/LJ, 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: The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Assistant DATES: PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 Published August 1, 2018. Administrator of the DEA Diversion Control Division (‘‘Assistant Administrator’’) pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.34(a), this is notice that on July 16, 2018, Cambrex High Point Inc., 4180 Mendenhall Oaks Parkway, High Point, North Carolina 27265–8017 applied to be registered as an importer of the following basic classes of controlled substances: Controlled substance Drug code Schedule Amphetamine ................... Codeine ............................ Oxymorphone ................... Noroxymorphone .............. 1100 9050 9652 9668 II II II II The company plans to manufacture the above listed controlled substances in bulk for distribution to its customers. Dated: October 1, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2018–22416 Filed 10–12–18; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Bulk Manufacturer of Controlled Substances Application: Specgx, LLC ACTION: Notice of application. Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written DATES: E:\FR\FM\15OCN1.SGM 15OCN1 51984 Federal Register / Vol. 83, No. 199 / Monday, October 15, 2018 / Notices comments on or objections to the issuance of the proposed registration on or before December 14, 2018. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Assistant Administrator of the DEA Diversion Control Division (‘‘Assistant Administrator’’) pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.33(a), this is notice that on July 26, 2018, Specgx, LLC, 3600 North Second Street, Saint Louis, Missouri 63147– 3457 applied to be registered as a bulk manufacturer of the following basic class of controlled substance: Drug code Controlled substance Fentanyl-related substances, their isomers, esters, ethers, salts and salts of isomers, esters, and ethers ................. The company plans to manufacture the above-listed controlled substance in gram quantities for sale as analytical research standards. Dated: September 24, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2018–22415 Filed 10–12–18; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF LABOR Agency Information Collection Activities; Submission for OMB Review; Comment Request; America’s Promise Job-Driven Grant Program Evaluation; Office of the Secretary Notice of availability; request for comments. ACTION: khammond on DSK30JT082PROD with NOTICES FOR FURTHER INFORMATION CONTACT: The Department of Labor (DOL) is submitting the information collection request (ICR) proposal titled, ‘‘E America’s Promise Job-Driven Grant Program Evaluation,’’ to the Office of Management and Budget (OMB) for review and approval for use in accordance with the Paperwork Reduction Act (PRA) of 1995. Public comments on the ICR are invited. DATES: The OMB will consider all written comments that agency receives on or before November 14, 2018. ADDRESSES: A copy of this ICR with applicable supporting documentation; including a description of the likely respondents, proposed frequency of response, and estimated total burden may be obtained free of charge from the RegInfo.gov website at http:// www.reginfo.gov/public/do/ PRAViewICR?ref_nbr=201801-1290-001 (this link will only become active on the day following publication of this notice) or by contacting Michel Smyth by telephone at 202–693–4129 (this is not SUMMARY: VerDate Sep<11>2014 21:34 Oct 12, 2018 Jkt 247001 a toll-free number) or by email at DOL_ PRA_PUBLIC@dol.gov. Submit comments about this request by mail to the Office of Information and Regulatory Affairs, Attn: OMB Desk Officer for DOL–OASP, Office of Management and Budget, Room 10235, 725 17th Street NW, Washington, DC 20503; by Fax: 202–395–5806 (this is not a toll-free number); or by email: OIRA_submission@omb.eop.gov. Commenters are encouraged, but not required, to send a courtesy copy of any comments by mail or courier to the U.S. Department of Labor-OASAM, Office of the Chief Information Officer, Attn: Departmental Information Compliance Management Program, Room N1301, 200 Constitution Avenue NW, Washington, DC 20210; or by email: DOL_PRA_PUBLIC@dol.gov. Michel Smyth by telephone at 202–693– 4129 (this is not a toll-free number) or by email at DOL_PRA_PUBLIC@dol.gov. This ICR seeks PRA authority for the America’s Promise Job-Driven Grant Program Evaluation information collection to support an implementation and impact evaluation. The America’s Promise program aims to create or expand regional partnerships that will identify the needs of specific industry sectors relying on the H–1B visa program to hire skilled foreign workers and prepare the domestic workforce for middle- and high-skilled, high-growth jobs in those sectors. This evaluation offers a unique opportunity to build knowledge about the implementation and effectiveness of these regional partnerships. The information collections consist of a grantee survey and a partner network survey. American Competitiveness and Workforce Improvement Act section 169 authorizes this information collection. See 29 U.S.C. 3224(a). SUPPLEMENTARY INFORMATION: PO 00000 Frm 00062 Fmt 4703 Sfmt 4703 Schedule 9850 I This proposed information collection is subject to the PRA. A Federal agency generally cannot conduct or sponsor a collection of information, and the public is generally not required to respond to an information collection, unless it is approved by the OMB under the PRA and displays a currently valid OMB Control Number. In addition, notwithstanding any other provisions of law, no person shall generally be subject to penalty for failing to comply with a collection of information if the collection of information does not display a valid Control Number. See 5 CFR 1320.5(a) and 1320.6. For additional information, see the related notice published in the Federal Register on July 12, 2017 (82 FR 32204). Interested parties are encouraged to send comments to the OMB, Office of Information and Regulatory Affairs at the address shown in the ADDRESSES section within thirty (30) days of publication of this notice in the Federal Register. In order to help ensure appropriate consideration, comments should mention OMB ICR Reference Number 201801–1290–001. The OMB is particularly interested in comments that: • 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, E:\FR\FM\15OCN1.SGM 15OCN1

Agencies

[Federal Register Volume 83, Number 199 (Monday, October 15, 2018)]
[Notices]
[Pages 51983-51984]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-22415]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Specgx, 
LLC

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and 
applicants therefore, may file written

[[Page 51984]]

comments on or objections to the issuance of the proposed registration 
on or before December 14, 2018.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: The Attorney General has delegated his 
authority under the Controlled Substances Act to the Administrator of 
the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority 
to exercise all necessary functions with respect to the promulgation 
and implementation of 21 CFR part 1301, incident to the registration of 
manufacturers, distributors, dispensers, importers, and exporters of 
controlled substances (other than final orders in connection with 
suspension, denial, or revocation of registration) has been redelegated 
to the Assistant Administrator of the DEA Diversion Control Division 
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, 
appendix to subpart R.
    In accordance with 21 CFR 1301.33(a), this is notice that on July 
26, 2018, Specgx, LLC, 3600 North Second Street, Saint Louis, Missouri 
63147-3457 applied to be registered as a bulk manufacturer of the 
following basic class of controlled substance:

------------------------------------------------------------------------
           Controlled substance               Drug code       Schedule
------------------------------------------------------------------------
Fentanyl-related substances, their                   9850  I
 isomers, esters, ethers, salts and salts
 of isomers, esters, and ethers.
------------------------------------------------------------------------

    The company plans to manufacture the above-listed controlled 
substance in gram quantities for sale as analytical research standards.

    Dated: September 24, 2018.
John J. Martin,
Assistant Administrator.
[FR Doc. 2018-22415 Filed 10-12-18; 8:45 am]
BILLING CODE 4410-09-P