[Federal Register Volume 61, Number 200 (Tuesday, October 15, 1996)]
[Notices]
[Pages 53761-53762]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-26320]


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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated June 27, 1996, and published in the Federal 
Register on July 5, 1996, (61 FR 35265), Dupont Pharmaceuticals, The 
Dupont Merck Pharmaceutical Company, 1000 Stewart Avenue, Garden City, 
New York 11530, made application to the Drug Enforcement Administration 
(DEA) for registration as a bulk manufacturer of the basic classes of 
controlled substances listed below:

[[Page 53762]]



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                    Drug                               Schedule         
------------------------------------------------------------------------
Oxycodone (9143)............................  II                        
Hydrocodone (9193)..........................  II                        
Oxymorphone (9652)..........................  II                        
------------------------------------------------------------------------

    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 Dupont Pharmaceuticals to 
manufacture the listed controlled substances is consistent with the 
public interest at this time. 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: September 25, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-26320 Filed 10-11-96; 8:45 am]
BILLING CODE 4410-09-M