[Federal Register Volume 59, Number 216 (Wednesday, November 9, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-27754]


[[Page Unknown]]

[Federal Register: November 9, 1994]


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DEPARTMENT OF JUSTICE
 

Manufacturer of Controlled Substances; Registration

    By Notice dated March 28, 1994, and published in the Federal 
Register on April 1, 1994, (59 FR 15458), Johnson Matthey, Inc., Custom 
Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey 
08066, made application to the Drug Enforcement Administration (DEA) to 
be registered as a bulk manufacturer of the basic classes of controlled 
substances listed below:

------------------------------------------------------------------------
                           Drug                               Schedule  
------------------------------------------------------------------------
2,5-dimethoxyamphetamine (7396)..........................  I            
Methylphenidate (1724)...................................  II           
Hydromorphone (9150).....................................  II           
Diphenoxylate (9170).....................................  II           
Meperidine (9230)........................................  II           
Morphine (9300)..........................................  II           
Alfentanil (9737)........................................  II           
Sufentanil (9740)........................................  II           
Carfentanil (9743).......................................  II           
Fentanyl (9801)..........................................  II           
------------------------------------------------------------------------

    A registered manufacturer did file a written request for a hearing 
with respect to Methylphenidate. Therefore, pursuant to section 303 of 
the Comprehensive Drug Abuse Prevention and Control Act of 1970 and 
Title 21, Code of Federal Regulations, Sec. 1301.54(e), 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 with the exception of Methylphenidate.

    Dated: November 3, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-27754 Filed 11-8-94; 8:45 am]
BILLING CODE 4410-09-M