Manufacturer of Controlled Substances; Notice of Application, 33476 [E9-16521]

Download as PDF 33476 Federal Register / Vol. 74, No. 132 / Monday, July 13, 2009 / Notices Landing Road, Wilmington, Delaware 19801, made application by letter to the Drug Enforcement Administration (DEA) to be registered as an importer of Thebaine (9333), a basic class of controlled substance listed in schedule II. The company plans to import a Thebaine derivative for the bulk manufacture of controlled substances for their customers. The company will also import analytical reference standards for distribution to their customers for research purposes. Any bulk manufacturer who is presently, or is applying to be, registered with DEA to manufacture such basic class of controlled substance 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 comments or objections being should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, VA 22152; and must be filed no later than August 12, 2009. 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 substances 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. Dated: July 1, 2009. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E9–16520 Filed 7–10–09; 8:45 am] mstockstill on DSKH9S0YB1PROD with NOTICES BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to § 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), VerDate Nov<24>2008 18:36 Jul 10, 2009 Jkt 217001 this is notice that on May 20, 2009, Organix Inc., 240 Salem Street, Woburn, Massachusetts 01801, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Marihuana (7360), a basic class of controlled substance listed in schedule I. The company plans to manufacture a synthetic cannabinol in bulk for sale to its customers for research purposes. No other activity for this drug code is authorized for this registration. 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). Any such written 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 September 11, 2009. Dated: July 1, 2009. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E9–16521 Filed 7–10–09; 8:45 am] BILLING CODE 4410–09–P NATIONAL AERONAUTICS AND SPACE ADMINISTRATION [Notice (09–066)] Review of U.S. Human Space Flight Plans Committee; Meeting AGENCY: National Aeronautics and Space Administration. ACTION: Notice of meeting. SUMMARY: In accordance with the Federal Advisory Committee Act, Public Law 92–463, as amended, the National Aeronautics and Space Administration announces a meeting of the Review of U.S. Human Space Flight Plans Committee. The agenda topics for the meeting include: • Kennedy Space Center Perspective. • Constellation projects. • Committee subgroup report. • Public comment. DATES: Thursday, July 30, 2009, 8 a.m.– 4 p.m. Note: All times listed are local times. ADDRESSES: Hilton Cocoa Beach Oceanfront, Grand Ballroom, 1550 North Atlantic Avenue, Cocoa Beach, Florida 32931, 321–799–0003. FOR FURTHER INFORMATION CONTACT: Mr. Philip R. McAlister, Office of Program PO 00000 Frm 00072 Fmt 4703 Sfmt 4703 Analysis and Evaluation, National Aeronautics and Space Administration, Washington, DC 20546. Phone 202–358– 0712. The meeting will be open to the public up to the seating capacity of the room. It is imperative that the meeting be held on this date to accommodate the scheduling priorities of the key participants. SUPPLEMENTARY INFORMATION: P. Diane Rausch, Advisory Committee Management Officer, National Aeronautics and Space Administration. [FR Doc. E9–16533 Filed 7–10–09; 8:45 am] BILLING CODE P NATIONAL AERONAUTICS AND SPACE ADMINISTRATION [Notice (09–064)] Review of U.S. Human Space Flight Plans Committee; Meeting AGENCY: National Aeronautics and Space Administration. ACTION: Notice of meeting. SUMMARY: In accordance with the Federal Advisory Committee Act, Public Law 92–463, as amended, the National Aeronautics and Space Administration announces a meeting of the Review of U.S. Human Space Flight Plans Committee. The agenda topics for the meeting include: • Johnson Space Center Perspective. • Constellation projects. • Committee subgroup report. • Public comment. DATES: Tuesday, July 28, 2009, 10 a.m.– 4 p.m. Note: All times listed are local times. ADDRESSES: South Shore Harbour Resort & Conference Center, Crystal Ballroom Salon A & B, 2500 South Shore Blvd., League City, TX 77573, 800–442–5005. FOR FURTHER INFORMATION CONTACT: Mr. Philip R. McAlister, Office of Program Analysis and Evaluation, National Aeronautics and Space Administration, Washington, DC 20546. Phone 202–358– 0712. The meeting will be open to the public up to the seating capacity of the room. It is imperative that the meeting be held on this date to accommodate the SUPPLEMENTARY INFORMATION: E:\FR\FM\13JYN1.SGM 13JYN1

Agencies

[Federal Register Volume 74, Number 132 (Monday, July 13, 2009)]
[Notices]
[Page 33476]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-16521]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec.  1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on May 20, 2009, Organix Inc., 
240 Salem Street, Woburn, Massachusetts 01801, made application by 
letter to the Drug Enforcement Administration (DEA) to be registered as 
a bulk manufacturer of Marihuana (7360), a basic class of controlled 
substance listed in schedule I.
    The company plans to manufacture a synthetic cannabinol in bulk for 
sale to its customers for research purposes. No other activity for this 
drug code is authorized for this registration.
    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).
    Any such written 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 September 11, 2009.

    Dated: July 1, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E9-16521 Filed 7-10-09; 8:45 am]
BILLING CODE 4410-09-P
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