[Federal Register Volume 63, Number 59 (Friday, March 27, 1998)]
[Notices]
[Page 14964]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-8085]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on February 6, 1998, Inhalon 
Pharmaceuticals, Inc., 3998 Schelden Circle, Bethlehem, Pennsylvania 
18017, made application to the Drug Enforcement Administration (DEA) 
for registration as a bulk manufacturer of the basic classes of 
controlled substances listed below:

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                    Drug                               Schedule         
------------------------------------------------------------------------
Amphetamine (1100).........................  II                         
Methylphenidate (1724).....................  II                         
------------------------------------------------------------------------

    The firm plans to develop a manufacturing process for these 
products such that the products can be ultimately formulated by the 
parent company.
    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 26, 1998.

    Dated: March 19, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-8085 Filed 3-26-98; 8:45 am]
BILLING CODE 4410-09-M