[Federal Register Volume 65, Number 28 (Thursday, February 10, 2000)]
[Notices]
[Page 6635]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 00-3146]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated October 8, 1999, and published in the Federal 
Register on October 18, 1999, (64 FR 56227), LifePoint, Inc., 10410 
Trademark Street, Rancho Cucamonga, California 91730, which has been 
changed to 10400 Trademark Street, Rancho Cucamonga, California 91730, 
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
------------------------------------------------------------------------
Tetrahydrocannabinols (7370)...............  I
Amphetamine (1100).........................  II
Methamphetamine (1105).....................  II
Phencyclidine (7471).......................  II
Benzoylecgonine (9180).....................  II
Morphine (9300)............................  II
------------------------------------------------------------------------

    The firms plans to use gram quantities of the listed controlled 
substances to manufacture drug abuse test kits.
    DEA has considered the factors in Title 21, United States Code, 
Section 823(a) and determined that the registration of LifePoint, Inc. 
to manufacture the listed controlled substances is consistent with the 
public interest at this time. DEA has investigated the firm 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: January 27, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 00-3146 Filed 2-9-00; 8:45 am]
BILLING CODE 4410-09-M