Manufacturer of Controlled Substances; Notice of Registration, 41841 [E6-11690]

Download as PDF Federal Register / Vol. 71, No. 141 / Monday, July 24, 2006 / Notices Dated: July 10, 2006. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E6–11690 Filed 7–21–06; 8:45 am] DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated March 20, 2006, and published in the Federal Register on March 27, 2006, (71 FR 15219), Organichem Corporation, 33 Riverside Avenue, Rensselaer, New York 12144, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in Schedules I and II: Drug Schedule sroberts on PROD1PC70 with NOTICES Marihuana (7360) ......................... Tetrahydrocannabinols (7370) ..... Amphetamine (1100) .................... Methylphenidate (1724) ................ Pentobarbital (2270) ..................... Hydrocodone (9193) ..................... Meperidine (9230) ........................ Dextropropoxyphene (9273) ......... Fentanyl (9801) ............................ I I II II II II II II II The company plans to manufacture bulk controlled substances for use in product development and for distribution to its customers. In reference to drug code 7360 (Marihuana), the company plans to bulk manufacture cannabindiol as a synthetic intermediate. This controlled substance will be further synthesized to bulk manufacture a synthetic THC (7370). No other activity for this drug code is authorized for this registration. No comments or objections have been received. DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Organichem Corporation to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Organichem Corporation to ensure that the company’s registration is consistent with the public interest. The investigation has included inspection and testing of the company’s physical security systems, verification of the company’s compliance with state and local laws, and a review of the company’s background and history. Therefore, pursuant to 21 U.S.C. 823, 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. VerDate Aug<31>2005 17:54 Jul 21, 2006 Jkt 208001 BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE National Institute of Corrections Advisory Board Meeting Time and Date: 8 a.m. to 4:30 p.m. on Monday, September 25, 2006. 8 a.m. to 4:30 p.m. on Tuesday, September 26, 2006. Place: Courtyard by Marriott Detroit, 333 E. Jefferson Avenue, Detroit, Michigan 48226, Phone: 313–222–7700. Status: Open. Matters to be Considered: Site Visit to Michigan Department of Corrections; Observation of Michigan Prisoner ReEntry Initiative; Faith Based; Evidence-based practices, Institutional culture work; and pubic/private funding partnerships; PREA Update; Agency Reports. For Further Information Contact: Larry Solomon, Deputy Director, 202– 307–3106, ext. 44254. Morris L. Thigpen, Director. [FR Doc. 06–6427 Filed 7–21–06; 8:45 am] BILLING CODE 4410–36–M DEPARTMENT OF LABOR Occupational Safety and Health Administration [Docket No. NRTL3–92] TUV Rheinland of North America, Inc., Application for Expansion of Recognition Occupational Safety and Health Administration (OSHA), Labor. ACTION: Notice. AGENCY: SUMMARY: This notice announces the application of TUV Rheinland of North America, Inc., (TUV) for expansion of its recognition to use additional test standards, and presents the Agency’s preliminary finding to grant this request for expansion. This preliminary finding does not constitute an interim or temporary approval of this application. DATES: You must submit information or comments, or any request for extension of the time to comment, by the following dates: • Hard copy: postmarked or sent by August 8, 2006. PO 00000 Frm 00088 Fmt 4703 Sfmt 4703 41841 • Electronic transmission or facsimile: sent by August 8, 2006. ADDRESSES: You may submit information or comments to this notice—identified by docket number NRTL3–92—by any of the following methods: • Federal eRulemaking Portal: https:// www.regulations.gov. Follow the instructions for submitting comments. • OSHA Web site: https:// ecomments.osha.gov. Follow the instructions for submitting comments on OSHA’s Web page. • Fax: If your written comments are 10 pages or fewer, you may fax them to the OSHA Docket Office at (202) 693– 1648. • Regular mail, express delivery, hand delivery and courier service: Submit three copies to the OSHA Docket Office, Docket No. NRTL3–92, U.S. Department of Labor, 200 Constitution Avenue, NW., Room N– 2625, Washington, DC 20210; telephone (202) 693–2350. (OSHA’s TTY number is (877) 889–5627). OSHA Docket Office hours of operation are 8:15 a.m. to 4:45 p.m., EST. Instructions: All comments received will be posted without change to https://dockets.osha.gov, including any personal information provided. OSHA cautions you about submitting personal information such as social security numbers and birth dates. Docket: For access to the docket to read background documents or comments received, go to https:// dockets.osha.gov. Contact the OSHA Docket Office for information about materials not available through the OSHA Web page and for assistance in using the Web page to locate docket submissions. Extension of Comment Period: Submit requests for extensions concerning this notice to the Office of Technical Programs and Coordination Activities, NRTL Program, Occupational Safety and Health Administration, U.S. Department of Labor, 200 Constitution Avenue, NW., Room N–3655, Washington, DC 20210. Or, fax to (202) 693–1644. FOR FURTHER INFORMATION CONTACT: Director, Office of Technical Programs and Coordination Activities, NRTL Program, Occupational Safety and Health Administration, U.S. Department of Labor, 200 Constitution Avenue, NW., Room N–3655, Washington, DC 20210, or phone (202) 693–2110. SUPPLEMENTARY INFORMATION: Notice of Application The Occupational Safety and Health Administration (OSHA) hereby gives notice that TUV Rheinland of North E:\FR\FM\24JYN1.SGM 24JYN1

Agencies

[Federal Register Volume 71, Number 141 (Monday, July 24, 2006)]
[Notices]
[Page 41841]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-11690]



[[Page 41841]]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated March 20, 2006, and published in the Federal 
Register on March 27, 2006, (71 FR 15219), Organichem Corporation, 33 
Riverside Avenue, Rensselaer, New York 12144, made application by 
renewal to the Drug Enforcement Administration (DEA) to be registered 
as a bulk manufacturer of the basic classes of controlled substances 
listed in Schedules I and II:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Marihuana (7360)...........................  I
Tetrahydrocannabinols (7370)...............  I
Amphetamine (1100).........................  II
Methylphenidate (1724).....................  II
Pentobarbital (2270).......................  II
Hydrocodone (9193).........................  II
Meperidine (9230)..........................  II
Dextropropoxyphene (9273)..................  II
Fentanyl (9801)............................  II
------------------------------------------------------------------------

    The company plans to manufacture bulk controlled substances for use 
in product development and for distribution to its customers. In 
reference to drug code 7360 (Marihuana), the company plans to bulk 
manufacture cannabindiol as a synthetic intermediate. This controlled 
substance will be further synthesized to bulk manufacture a synthetic 
THC (7370). No other activity for this drug code is authorized for this 
registration.
    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. 823(a) and determined that the registration of 
Organichem Corporation to manufacture the listed basic classes of 
controlled substances is consistent with the public interest at this 
time. DEA has investigated Organichem Corporation to ensure that the 
company's registration is consistent with the public interest. The 
investigation has included inspection and testing of the company's 
physical security systems, verification of the company's compliance 
with state and local laws, and a review of the company's background and 
history. Therefore, pursuant to 21 U.S.C. 823, 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.

     Dated: July 10, 2006.
 Joseph T. Rannazzisi,
 Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
 [FR Doc. E6-11690 Filed 7-21-06; 8:45 am]
BILLING CODE 4410-09-P
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