99-11448. Manufacturer of Controlled Substances; Notice of Registration  

  • [Federal Register Volume 64, Number 88 (Friday, May 7, 1999)]
    [Notices]
    [Page 24679]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 99-11448]
    
    
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    DEPARTMENT OF JUSTICE
    
    Drug Enforcement Administration
    
    
    Manufacturer of Controlled Substances; Notice of Registration
    
        By Notice dated January 27, 1999, and published in the Federal 
    Register on February 4, 1999, (64 FR 5689), Orpharm, Inc., 4815 Dacoma, 
    Houston, Texas 77072, 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
    ------------------------------------------------------------------------
    Methadone (9250)...........................  II
    Methadone-intermediate (9254)..............  II
    levo-alphacetylmethadol (9648).............  II
    ------------------------------------------------------------------------
    
        The firm plans to manufacture methadone and methadone-intermediate 
    for production of LAAM.
        DEA has considered the factors in 21 U.S.C. Sec. 823(a) and 
    determined that the registration of Orpharm, Inc. to manufacture the 
    listed controlled substances is consistent with the public interest at 
    this time. DEA has investigated Orpharm, 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 C.F.R. 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: April 26, 1999.
    John H. King,
    Deputy Assistant Administrator, Office of Diversion Control, Drug 
    Enforcement Administration.
    [FR Doc. 99-11448 Filed 5-6-99; 8:45 am]
    BILLING CODE 4410-09-M
    
    
    

Document Information

Published:
05/07/1999
Department:
Drug Enforcement Administration
Entry Type:
Notice
Document Number:
99-11448
Pages:
24679-24679 (1 pages)
PDF File:
99-11448.pdf