Manufacturer of Controlled Substances; Notice of Application, 33785 [2011-14253]

Download as PDF Federal Register / Vol. 76, No. 111 / Thursday, June 9, 2011 / Notices The company plans to import these controlled substances for the manufacture of reference standards. Any bulk manufacturer who is presently, or is applying to be, registered with DEA to manufacture such basic classes of controlled substances may file comments or objections to the issuance of the proposed registration and may, at the same time, file a written request for a hearing on such application pursuant to 21 CFR 1301.43, and in such form as prescribed by 21 CFR 1316.47. Any such written comments or objections should be addressed, in quintuplicate, to Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than July 11, 2011. This procedure is to be conducted simultaneously with, and independent of, the procedures described in 21 CFR 1301.34(b), (c), (d), (e), and (f). As noted in a previous notice published in the Federal Register on September 23, 1975, 40 FR 43745–46, all applicants for registration to import a basic class of any controlled substance in Schedule I or II are, and will continue to be, required to demonstrate to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, that the requirements for such registration pursuant to 21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR 1301.34(b), (c), (d), (e), and (f) are satisfied. Drug I I Any such comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later than August 8, 2011. I I I I Dated: June 1, 2011. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. Schedule Manufacturer of Controlled Substances; Notice of Application Methcathinone (1237) .................. N-ethylamphetamine (1475) ......... N,N-dimethylamphetamine (1480) 4-methylaminorex (cis isomer) (1590). Alpha-ethyltryptamine (7249) ....... Lysergic acid diethylamide (7315) 2,5-dimethoxy-4-(n)propylthiophenethylamine. (7348) ........................................... Tetrahydrocannabinols (7370) ..... Mescaline (7381) .......................... 4-bromo-2,5-dimethoxy-amphetamine (7391). 4–Bromo-2,5dimethoxyphenethylamine (7392). 4-methyl-2,5-dimethoxy-amphetamine (7395). 2,5-dimethoxyamphetamine (7396). 2,5-dimethoxy-4ethylamphetamine (7399). 3,4-methylenedioxy amphetamine (7400). N-hydroxy-3,4methylenedioxyamphetamine (7402). 3,4-methylenedioxy-Nethylamphetamine (7404). 3,4methylenedioxymethamphetamine (MDMA) (7405). 4-methoxyamphetamine (7411) ... Alpha-methyltryptamine (7432) .... Bufotenine (7433) ......................... Diethyltryptamine (7434) .............. Dimethyltryptamine (7435) ........... Psilocybin (7437) .......................... Psilocyn (7438) ............................. 5-methoxy-N,Ndiisopropyltryptamine (7439). N-ethyl-1-phenylcyclohexylamine (7455). 1-(1-phenylcyclohexyl)-pyrrolidine (7458). 1-[1-(2-thienyl)-cyclohexyl]-piperidine (7470). Dihydromorphine (9145) ............... Normorphine (9313) ..................... Methamphetamine (1105) ............ 1-phenylcyclohexylamine (7460) .. Phencyclidine (7471) .................... Phenylacetone (8501) .................. 1-piperidinocyclohexanecarbonitrile (8603). Cocaine (9041) ............................. Codeine (9050) ............................. Dihydrocodeine (9120) ................. Ecgonine (9180) ........................... Meperidine intermediate-B (9233) Noroxymorphone (9668) .............. Pursuant to § 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on March 28, 2011, Alltech Associates Inc., 2051 Waukegan Road, Deerfield, Illinois 60015, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the following basic classes of controlled substances: The company plans to manufacture high purity drug standards used for analytical applications only in clinical, toxicological, and forensic laboratories. Any other such applicant, and any person who is presently registered with DEA to manufacture such substances, may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR § 1301.33(a). Dated: June 1, 2011. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2011–14255 Filed 6–8–11; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE mstockstill on DSK4VPTVN1PROD with NOTICES Drug Enforcement Administration VerDate Mar<15>2010 19:07 Jun 08, 2011 Jkt 223001 PO 00000 Frm 00086 Fmt 4703 Sfmt 4703 33785 I I I I [FR Doc. 2011–14253 Filed 6–8–11; 8:45 am] I BILLING CODE 4410–09–P I DEPARTMENT OF JUSTICE I Federal Bureau of Investigation I Notice of Charter Reestablishment I In accordance with the provisions of the Federal Advisory Committee Act, Title 5, United States Code, Appendix, and Title 41, Code of Federal Regulations, Section 101–6.1015, with the concurrence of the Attorney General, I have determined that the reestablishment of the Criminal Justice Information Services (CJIS) Advisory Policy Board (APB) is in the public interest. In connection with the performance of duties imposed upon the FBI by law, I hereby give notice of the reestablishment of the APB Charter. The APB provides me with general policy recommendations with respect to the philosophy, concept, and operational principles of the various criminal justice information systems managed by the FBI’s CJIS Division. The APB includes representatives from local and state criminal justice agencies; Tribal law enforcement representatives; members of the judicial, prosecutorial, and correctional sectors of the criminal justice community, as well as one individual representing a national security agency; a representative of Federal agencies participating in the CJIS Division Systems; and representatives of criminal justice professional associations (i.e., the American Probation and Parole Association; American Society of Crime Laboratory Directors, Inc.; International Association of Chiefs of Police; National District Attorneys’ Association; National Sheriffs’ Association; Major Cities Chiefs’ Association; Major County Sheriffs’ Association; and a representative from a national professional association representing the courts or court administrators nominated by the Conference of Chief Justices). The Attorney General has I I I I I I I I I I I I I I I I II II II II II II II II II II II E:\FR\FM\09JNN1.SGM 09JNN1

Agencies

[Federal Register Volume 76, Number 111 (Thursday, June 9, 2011)]
[Notices]
[Page 33785]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-14253]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec.  1301.33(a), Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on March 28, 2011, Alltech 
Associates Inc., 2051 Waukegan Road, Deerfield, Illinois 60015, made 
application by renewal to the Drug Enforcement Administration (DEA) to 
be registered as a bulk manufacturer of the following basic classes of 
controlled substances:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Methcathinone (1237).......................  I
N-ethylamphetamine (1475)..................  I
N,N-dimethylamphetamine (1480).............  I
4-methylaminorex (cis isomer) (1590).......  I
Alpha-ethyltryptamine (7249)...............  I
Lysergic acid diethylamide (7315)..........  I
2,5-dimethoxy-4-(n)-
 propylthiophenethylamine.
(7348).....................................  I
Tetrahydrocannabinols (7370)...............  I
Mescaline (7381)...........................  I
4-bromo-2,5-dimethoxy-amphetamine (7391)...  I
4-Bromo-2,5-dimethoxyphenethylamine (7392).  I
4-methyl-2,5-dimethoxy-amphetamine (7395)..  I
2,5-dimethoxyamphetamine (7396)............  I
2,5-dimethoxy-4-ethylamphetamine (7399)....  I
3,4-methylenedioxy amphetamine (7400)......  I
N-hydroxy-3,4-methylenedioxyamphetamine      I
 (7402).
3,4-methylenedioxy-N-ethylamphetamine        I
 (7404).
3,4-methylenedioxymethamphetamine (MDMA)     I
 (7405).
4-methoxyamphetamine (7411)................  I
Alpha-methyltryptamine (7432)..............  I
Bufotenine (7433)..........................  I
Diethyltryptamine (7434)...................  I
Dimethyltryptamine (7435)..................  I
Psilocybin (7437)..........................  I
Psilocyn (7438)............................  I
5-methoxy-N,N-diisopropyltryptamine (7439).  I
N-ethyl-1-phenylcyclohexylamine (7455).....  I
1-(1-phenylcyclohexyl)-pyrrolidine (7458)..  I
1-[1-(2-thienyl)-cyclohexyl]-piperidine      I
 (7470).
Dihydromorphine (9145).....................  I
Normorphine (9313).........................  I
Methamphetamine (1105).....................  II
1-phenylcyclohexylamine (7460).............  II
Phencyclidine (7471).......................  II
Phenylacetone (8501).......................  II
1-piperidinocyclohexane-carbonitrile (8603)  II
Cocaine (9041).............................  II
Codeine (9050).............................  II
Dihydrocodeine (9120)......................  II
Ecgonine (9180)............................  II
Meperidine intermediate-B (9233)...........  II
Noroxymorphone (9668)......................  II
------------------------------------------------------------------------

    The company plans to manufacture high purity drug standards used 
for analytical applications only in clinical, toxicological, and 
forensic laboratories.
    Any other such applicant, and any person who is presently 
registered with DEA to manufacture such substances, may file comments 
or objections to the issuance of the proposed registration pursuant to 
21 CFR Sec.  1301.33(a).
    Any such comments or objections should be addressed, in 
quintuplicate, to the Drug Enforcement Administration, Office of 
Diversion Control, Federal Register Representative (ODL), 8701 
Morrissette Drive, Springfield, Virginia 22152; and must be filed no 
later than August 8, 2011.

    Dated: June 1, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 2011-14253 Filed 6-8-11; 8:45 am]
BILLING CODE 4410-09-P
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