99-7941. Manufacturer of Controlled Substances; Notice of Registration  

  • [Federal Register Volume 64, Number 62 (Thursday, April 1, 1999)]
    [Notices]
    [Page 15809]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-7941]
    
    
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    DEPARTMENT OF JUSTICE
    
    Drug Enforcement Administration
    
    
    Manufacturer of Controlled Substances; Notice of Registration
    
        By Notice dated October 1, 1998, and published in the Federal 
    Register on October 9, 1998, (63 FR 54492), Nycomed, Inc., 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 
    below:
    
    ------------------------------------------------------------------------
                        Drug                               Schedule
    ------------------------------------------------------------------------
    Methylphenidate (1724).....................  II
    Meperidine (9230)..........................  II
    ------------------------------------------------------------------------
    
        The firm plans to manufacture meperidine as bulk product for 
    distribution to it customers and to perform a chemical isolation 
    process on methylphenidate which has been manufactured by another bulk 
    manufacturer of methylphenidate.
        DEA has considered the factors in Title 21, United States Code, 
    section 823(a) and determined that the registration of Nycomed, Inc. to 
    manufacture the listed controlled substances is consistent with the 
    public interest at this time. DEA has investigated Mycomed, Inc. on a 
    regular basis to ensure that the company's continued registration is 
    consistent with the public interest. These investigations have included 
    inspection and testing of the company's physical security systems, 
    audits of the company's records, 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 28 CFR 
    0.100 and 0.104, the Deputy Assistant Administrator, Office of 
    Diversion Control, hereby orders that the application submitted by the 
    above firm for registration as a bulk manufacturer of the basic classes 
    of controlled substances listed above is granted.
    
        Dated: March 1, 1999.
    John H. King,
    Deputy Assistant Administrator, Office of Diversion Control, Drug 
    Enforcement Administration.
    [FR Doc. 99-7941 Filed 3-31-99; 8:45 am]
    BILLING CODE 4410-09-M
    
    
    

Document Information

Published:
04/01/1999
Department:
Drug Enforcement Administration
Entry Type:
Notice
Document Number:
99-7941
Pages:
15809-15809 (1 pages)
PDF File:
99-7941.pdf