[Federal Register Volume 63, Number 44 (Friday, March 6, 1998)]
[Notices]
[Page 11310]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-5757]


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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 January 12, 1998, Johnson 
Matthey, Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, 
West Deptford, New Jersey 08066, made application by renewal to the 
Drug Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

------------------------------------------------------------------------
                    Drug                               Schedule         
------------------------------------------------------------------------
Difenoxin (9168)...........................  I                          
Propiram (9649)............................  I                          
Amphetamine (1100).........................  II                         
Methylphenidate (1724).....................  II                         
Phenylacetone (8501).......................  II                         
Dihydrocodeine (9120)......................  II                         
Oxycodone (9143)...........................  II                         
Hydromorphone (9150).......................  II                         
Hydrocodone (9193).........................  II                         
Meperidine (9230)..........................  II                         
Thebaine (9333)............................  II                         
Alfentanil (9737)..........................  II                         
Sufentanil (9740)..........................  II                         
Carfentanil (9743).........................  II                         
Fentanyl (9801)............................  II                         
------------------------------------------------------------------------

    The firm plans to manufacture the listed controlled substances in 
bulk to supply final dosage form manufacturers.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substances 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, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than May 5, 1998.

    Dated: February 24, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-5757 Filed 3-5-98; 8:45 am]
BILLING CODE 4410-09-M