[Federal Register: January 4, 1999 (Volume 64, Number 1)]
[Notices]               
[Page 181-182]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04ja99-95]

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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

[[Page 182]]

9, 1998, Knoll Pharmaceutical Company, 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
------------------------------------------------------------------------
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 substance 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 March 5, 1999.

    Dated: December 23, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 98-34812 Filed 12-31-98; 8:45 am]
BILLING CODE 4410-09-M