[Federal Register Volume 60, Number 159 (Thursday, August 17, 1995)]
[Notices]
[Page 42904]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-20336]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated May 30, 1995, and published in the Federal Register 
on June 8, 1995, (60 FR 30320), Johnson & Johnson Pharmaceutical 
Partners, HC02 State Road 933, KMO.1 Mamey Ward, HC-02 Box 19250, 
Gurabo, Puerto Rico 00778-9629, made application to the Drug 
Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

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                             Drug                               Schedule
------------------------------------------------------------------------
Alfentanil (9737).............................................  II      
Sufentanil (9740).............................................  II      
------------------------------------------------------------------------

    No comments or objections have been received. Therefore, pursuant 
to Section 303 of the Comprehensive Drug Abuse Prevention and Control 
Act of 1970 and Title 21, Code of Federal Regulations, Section 
1301.54(e), the Deputy Assistant Administrator, Office of Division 
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: August 10, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-20336 Filed 8-16-95; 8:45 am]
BILLING CODE 4410-09-M