Manufacturer of Controlled Substances Registration: American Radiolabeled Chemicals, Inc., 45551-45552 [2015-18692]

Download as PDF 45551 Federal Register / Vol. 80, No. 146 / Thursday, July 30, 2015 / Notices The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Cambridge Isotope Lab to manufacture the basic class of controlled substance 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 the 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. 823(a), and in accordance with 21 CFR 1301.33, the above-named company is granted registration as a bulk manufacturer of morphine (9300), a basic class of controlled substance listed in schedule II. The company plans to utilize small quantities of the listed controlled substance in the preparation of analytical standards. Dated: July 23, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015–18693 Filed 7–29–15; 8:45 am] BILLING CODE 4410–09P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Registration: Stepan Company ACTION: Dated: July 23, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. Notice of registration. Stepan Company applied to be registered as an importer of certain basic class of controlled substances. The Drug Enforcement Administration (DEA) grants Stepan Company registration as an importer of this controlled substance. SUPPLEMENTARY INFORMATION: By notice dated April 14, 2015, and published in SUMMARY: the Federal Register on April 22, 2015, 80 FR 22561, Stepan Company, Natural Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607 applied to be registered as an importer of a certain basic class of controlled substance. Comments and request for hearings on applications to import narcotic raw material are not appropriate. 72 FR 3417 (January 25, 2007). The DEA has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of Stepan Company to import the basic class of controlled substance 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 the 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 above-named company is granted registration as an importer of coca leaves (9040) a basic class of controlled substance listed in schedule II. The company plans to import the listed controlled substance to manufacture bulk controlled substances for distribution to its customers. [FR Doc. 2015–18691 Filed 7–29–15; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Manufacturer of Controlled Substances Registration: American Radiolabeled Chemicals, Inc. ACTION: Notice of registration. American Radiolabeled Chemicals, Inc. applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants American Radiolabeled Chemicals, Inc. registration as a manufacturer of those controlled substances. SUMMARY: By notice dated January 28, 2015, and published in the Federal Register on February 5, 2015, 80 FR 6547, American Radiolabeled Chemicals, Inc., 101 Arc Drive, St. Louis, Missouri 63146 applied to be registered as a manufacturer of certain basic classes of controlled substances. No comments or objections were submitted to this notice. The DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of American Radiolabeled Chemicals, Inc. to manufacture the basic classes of 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 the 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. 823(a), and in accordance with 21 CFR 1301.33, the above-named company is granted registration as a bulk manufacturer of the basic classes of controlled substances listed: SUPPLEMENTARY INFORMATION: Lhorne on DSK7TPTVN1PROD with NOTICES Controlled substance Schedule Gamma Hydroxybutyric Acid (2010) ........................................................................................................................................................... Ibogaine (7260) ........................................................................................................................................................................................... Lysergic Acid Diethylamide (7315) .............................................................................................................................................................. Tetrahydrocannabinols (7370) ..................................................................................................................................................................... Dimethyltryptamine (7435) .......................................................................................................................................................................... 1-[1-(2-Thienyl)cyclohexyl]piperidine (7470) ............................................................................................................................................... Dihydromorphine (9145) .............................................................................................................................................................................. Heroin (9200) ............................................................................................................................................................................................... Normorphine (9313) .................................................................................................................................................................................... Amphetamine (1100) ................................................................................................................................................................................... Methamphetamine (1105) ........................................................................................................................................................................... Amobarbital (2125) ...................................................................................................................................................................................... Phencyclidine (7471) ................................................................................................................................................................................... VerDate Sep<11>2014 14:54 Jul 29, 2015 Jkt 235001 PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 E:\FR\FM\30JYN1.SGM 30JYN1 I I I I I I I I I II II II II 45552 Federal Register / Vol. 80, No. 146 / Thursday, July 30, 2015 / Notices Controlled substance Schedule Phenylacetone (8501) ................................................................................................................................................................................. Cocaine (9041) ............................................................................................................................................................................................ Codeine (9050) ............................................................................................................................................................................................ Dihydrocodeine (9120) ................................................................................................................................................................................ Oxycodone (9143) ....................................................................................................................................................................................... Hydromorphone (9150) ............................................................................................................................................................................... Ecgonine (9180) .......................................................................................................................................................................................... Hydrocodone (9193) .................................................................................................................................................................................... Meperidine (9230) ....................................................................................................................................................................................... Metazocine (9240) ....................................................................................................................................................................................... Methadone (9250) ....................................................................................................................................................................................... Dextropropoxyphene, bulk (non-dosage forms) (9273) .............................................................................................................................. Morphine (9300) .......................................................................................................................................................................................... Oripavine (9330) .......................................................................................................................................................................................... Thebaine (9333) .......................................................................................................................................................................................... Oxymorphone (9652) ................................................................................................................................................................................... Phenazocine (9715) .................................................................................................................................................................................... Carfentanil (9743) ........................................................................................................................................................................................ Fentanyl (9801) ........................................................................................................................................................................................... The company plans to manufacture small quantities of the listed controlled substances as radiolabeled compounds for biochemical research. Dated: July 23, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015–18692 Filed 7–29–15; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Registration: Pharmacore ACTION: Notice of registration. Pharmacore applied to be registered as an importer of a certain basic class of controlled substance. The Drug Enforcement Administration (DEA) grants Pharmacore registration as an importer of this controlled substance. SUPPLEMENTARY INFORMATION: By notice dated April 14, 2015, and published in the Federal Register on April 22, 2015, 80 FR 22553, Pharmacore, 4180 Mendenhall Oaks Parkway, High Point, North Carolina 27265 applied to be registered as an importer of a certain basic class of controlled substance. Comments and request for hearings on applications to import narcotic raw material are not appropriate. 72 FR 3417 (January 25, 2007). The DEA has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of Pharmacore to import the basic class of controlled substance is consistent with the public interest and with United States obligations under international treaties, conventions, or protocols in Lhorne on DSK7TPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 14:54 Jul 29, 2015 Jkt 235001 effect on May 1, 1971. The DEA investigated the company’s maintenance of effective controls against diversion by inspecting and testing the 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 above-named company is granted registration as an importer of poppy straw concentrate (9670), a basic class of controlled substance listed in schedule II. The company plans to import the listed controlled substance to manufacture bulk controlled substance intermediates for sale to its customers. Dated: July 23, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015–18690 Filed 7–29–15; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE [OMB Number 1110—NEW] Agency Information Collection Activities;Proposed eCollection eComments Requested; Approval of an Existing Collection in Use Without an OMB Control Number; Records Modification Form (FD–1115) Federal Bureau of Investigation, Department of Justice. ACTION: 30-day notice. AGENCY: The Department of Justice (DOJ), Federal Bureau of Investigation (FBI), Criminal Justice Information Services (CJIS) Division will be submitting the following information collection request to the Office of Management and Budget (OMB) for SUMMARY: PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 II II II II II II II II II II II II II II II II II II II review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection was previously published in the 80 FR 30269, on May 27, 2015, allowing for a 60 day comment period. DATES: Comments are encouraged and will be accepted for an additional 30 days until August 31, 2015. FOR FURTHER INFORMATION CONTACT: If you have 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 the Office of Management and Budget, Office of Information and Regulatory Affairs, Attention Department of Justice Desk Officer, Washington, DC, 20503. Additionally, comments may be submitted via email to OIRA_submission@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 E:\FR\FM\30JYN1.SGM 30JYN1

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[Federal Register Volume 80, Number 146 (Thursday, July 30, 2015)]
[Notices]
[Pages 45551-45552]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-18692]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Manufacturer of Controlled Substances Registration: American 
Radiolabeled Chemicals, Inc.

ACTION: Notice of registration.

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

SUMMARY: American Radiolabeled Chemicals, Inc. applied to be registered 
as a manufacturer of certain basic classes of controlled substances. 
The Drug Enforcement Administration (DEA) grants American Radiolabeled 
Chemicals, Inc. registration as a manufacturer of those controlled 
substances.

SUPPLEMENTARY INFORMATION: By notice dated January 28, 2015, and 
published in the Federal Register on February 5, 2015, 80 FR 6547, 
American Radiolabeled Chemicals, Inc., 101 Arc Drive, St. Louis, 
Missouri 63146 applied to be registered as a manufacturer of certain 
basic classes of controlled substances. No comments or objections were 
submitted to this notice.
    The DEA has considered the factors in 21 U.S.C. 823(a) and 
determined that the registration of American Radiolabeled Chemicals, 
Inc. to manufacture the basic classes of 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 the 
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. 823(a), and in accordance with 21 
CFR 1301.33, the above-named company is granted registration as a bulk 
manufacturer of the basic classes of controlled substances listed:

------------------------------------------------------------------------
            Controlled substance                       Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid (2010)............  I
Ibogaine (7260).............................  I
Lysergic Acid Diethylamide (7315)...........  I
Tetrahydrocannabinols (7370)................  I
Dimethyltryptamine (7435)...................  I
1-[1-(2-Thienyl)cyclohexyl]piperidine (7470)  I
Dihydromorphine (9145)......................  I
Heroin (9200)...............................  I
Normorphine (9313)..........................  I
Amphetamine (1100)..........................  II
Methamphetamine (1105)......................  II
Amobarbital (2125)..........................  II
Phencyclidine (7471)........................  II

[[Page 45552]]

 
Phenylacetone (8501)........................  II
Cocaine (9041)..............................  II
Codeine (9050)..............................  II
Dihydrocodeine (9120).......................  II
Oxycodone (9143)............................  II
Hydromorphone (9150)........................  II
Ecgonine (9180).............................  II
Hydrocodone (9193)..........................  II
Meperidine (9230)...........................  II
Metazocine (9240)...........................  II
Methadone (9250)............................  II
Dextropropoxyphene, bulk (non-dosage forms)   II
 (9273).
Morphine (9300).............................  II
Oripavine (9330)............................  II
Thebaine (9333).............................  II
Oxymorphone (9652)..........................  II
Phenazocine (9715)..........................  II
Carfentanil (9743)..........................  II
Fentanyl (9801).............................  II
------------------------------------------------------------------------

    The company plans to manufacture small quantities of the listed 
controlled substances as radiolabeled compounds for biochemical 
research.

    Dated: July 23, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2015-18692 Filed 7-29-15; 8:45 am]
 BILLING CODE P