[Federal Register Volume 64, Number 248 (Tuesday, December 28, 1999)]
[Notices]
[Page 72685]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-33649]


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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 September 9, 1999, Knoll 
Pharmaceuticals, 30 North Jefferson Road, Whippany, New Jersey 07981, 
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:

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                   Drug                               Schedule
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Dihydromorphine (9145)....................  I
Hydromorphone (9150)......................  II
------------------------------------------------------------------------

    The firm plans to produce bulk product and finished dosage units 
for distribution to its customers.
    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 objectives may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than February 28, 2000.

    Dated: December 16, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-33649 Filed 12-27-99; 8:45 am]
BILLING CODE 4410-09-M