05-67. Manufacturer of Controlled Substances; Notice of Application  

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    Pursuant to 21 CFR 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on September 2, 2004, Organix Inc., 240 Salem Street, Woburn, Massachusetts 01801, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of Codeine (9041), a basic class of controlled substance listed in Schedule II.

    The company plans to manufacture small quantities of the listed controlled substance for use in drug abuse detection kits.

    Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a).

    Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: DEA Federal Register Representative, Office of Liaison and Policy (ODLR) and must be filed no later than March 7, 2005.

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    Dated: December 21, 2004.

    William J. Walker,

    Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

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    [FR Doc. 05-67 Filed 1-3-05; 8:45 am]

    BILLING CODE 4410-09-P

Document Information

Published:
01/04/2005
Department:
Drug Enforcement Administration
Entry Type:
Notice
Document Number:
05-67
Pages:
393-393 (1 pages)
PDF File:
05-67.pdf