[Federal Register: September 29, 2006 (Volume 71, Number 189)]
[Notices]
[Page 57570]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29se06-125]
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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 May 30, 2006, Abbott
Laboratories, DBA Knoll Pharmaceutical Company, 30 North Jefferson
Road, Whippany, New Jersey, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as a bulk
manufacturer of the basic classes of controlled substances listed in
Schedules I and II:
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Drug Schedule
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Dihydromorphine (9145)..................... I
Hydromorphone (9150)....................... II
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The company plans to manufacture bulk product and dosage units for
distribution to its customers.
Any other such applicant and any person who is presently registered
with DEA to manufacture such a substance may file comments or
objections to the issuance of the proposed registration pursuant to 21
CFR 1301.33(a).
Any such written comments or objections being sent via regular mail
should be addressed, in quintuplicate, to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537, Attention: DEA Federal Register
Representative/ODL; or any being sent via express mail should be sent
to DEA Headquarters, Attention: DEA Federal Register Representative/
ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must
be filed no later than November 28, 2006.
Dated: September 20, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E6-16032 Filed 9-28-06; 8:45 am]
BILLING CODE 4410-09-P