[Federal Register: October 14, 2008 (Volume 73, Number 199)]
[Notices]
[Page 60719]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr14oc08-80]
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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 May 13, 2008, Halo
Pharmaceutical Inc., 30 North Jefferson Road, Whippany, New Jersey
07981, made application 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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Dihydromorphine is an intermediate in the manufacture of
Hydromorphone and is not for commercial distribution. The company plans
to manufacture Hydromorphone HCL for sale to other manufacturers and
for the manufacture of other controlled substance 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 pursuant to
21 CFR 1301.33(a).
Any such written comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than December 15, 2008.
Dated: October 7, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-24310 Filed 10-10-08; 8:45 am]
BILLING CODE 4410-09-P