Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Application - 2000

[Federal Register: May 12, 2000 (Volume 65, Number 93)] [Notices] [Page 30615] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr12my00-118]


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 March 21, 2000, Lifepoint, Inc., 10410 Trademark Street, Rancho Cucamonga, California 91730, made application by renewal to the Drug Enforcement Administration (DEA) for the 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 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, D.C. 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than July 11, 2000.

Dated: April 21, 2000.

John H. King,
Deputy Assistant Administrator Office of Diversion Control Drug Enforcement Administration.

[FR Doc. 00-11888 Filed 5-11-00; 8:45 am]

BILLING CODE 4410-09-M

 

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