[Federal Register Volume 64, Number 200 (Monday, October 18, 1999)]
[Notices]
[Page 56227]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-27103]


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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 February 22, 1999, Lifepoint, 
Inc., 10410 Trademark Street, Rancho Cucamonga, California 91730, made 
application by renewal to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of the basic classes of controlled 
substances listed below:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)...............  I
Amphetamine (1100).........................  II
Methamphetamine (1105).....................  II
Phencyclidine (7471).......................  II
Benzoylecgonine (9180).....................  II
Morphine (9300)............................  II
------------------------------------------------------------------------

    The firm plans to use gram quantities of the listed controlled 
substances to manufacture drug abuse test kits.
    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 November 17, 1999.

    Dated: October 8, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-27103 Filed 10-15-99; 8:45 am]
BILLING CODE 4410-09-M