[Federal Register Volume 64, Number 197 (Wednesday, October 13, 1999)]
[Notices]
[Page 55490]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-26606]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on August 9, 1999, Irix 
Pharmaceuticals, Inc., 101 Technology Place, Florence, South Carolina 
29501, made application by renewal to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of 
methylphenidate (1724), a basic class of controlled substance listed in 
Schedule II.
    The firm plans to manufacture methylphenidate for demonstration 
purposes and for dosage form development and stability studies.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substance may file comments or objections 
to the issuance of the proposed registration.
    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 
(CCR), and must be filed no later than December 13, 1999.

    Dated: October 1, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control Drug 
Enforcement Administration.
[FR Doc. 99-26606 Filed 10-12-99; 8:45 am]
BILLING CODE 4410-09-M