[Federal Register Volume 63, Number 186 (Friday, September 25, 1998)]
[Notices]
[Page 51374]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-25654]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated May 6, 1998, and published in the Federal Register 
on May 19, 1998, (63 FR 27587), High Standard Products, 1100 W. 
Florence Avenue, #B, Inglewood, California 90301, made application by 
letter to the Drug Enforcement Administration (DEA) to be registered as 
a bulk manufacturer of normorphine (9313), a basic class of controlled 
substance listed in Schedule I.
    The firms plans to manufacture an analytical reference standard.
    No comments or objections have been received. DEA has considered 
the factors in Title 21, United States Code, Section 823(a) and 
determined that the registration of High Standard Products to 
manufacture the listed controlled substances is consistent with the 
public interest at this time. DEA has investigated High Standard 
Products 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 class of controlled substance listed above is 
granted.

    Dated: September 11, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-25654 Filed 9-24-98; 8:45 am]
BILLING CODE 4410-09-M