[Federal Register Volume 61, Number 248 (Tuesday, December 24, 1996)]
[Notices]
[Page 67853]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-32606]
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DEPARTMENT OF JUSTICE
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated August 21, 1996, and published in the Federal
Register on September 5, 1996, (61 FR 46827), Noramco of Delaware,
Inc., Division of McNeilab, Inc., 500 Old Swedes Landing Road,
Wilmington, Delaware 19801, made application for 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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Codeine (9050).............................................. II
Oxycodone (9143)............................................ II
Hydrocodone (9193).......................................... II
Morphine (9300)............................................. II
Thebaine (9333)............................................. II
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By a Notice of Correction dated October 21, 1996, and published in
the Federal Register on November 14, 1996, (61 FR 58424), fentanyl was
deleted from Noramco of Delaware, Inc.'s application for bulk
manufacture.
No comments or objections have been received. DEA has considered
the factors in Title 21, United States Code, Section 823(a) and
determined that the registration of Noramco of Delaware, Inc. to
manufacture the listed controlled substances is consistent with the
public interest at this time. Therefore, pursuant to 21 U.S.C. 823 and
28 C.F.R. 0.100 and 0.104, the Deputy Assistant Administrator, Office
of Diversion Control, hereby orders that the application submitted by
the above firm for registration as a bulk manufacturer of the basic
classes of controlled substances listed above is granted, except for
fentanyl.
Dated: December 5, 1996.
Gene R. Haislip,
Deputy Assistant Administrator Office of Diversion Control Drug
Enforcement Administration.
[FR Doc. 96-32606 Filed 12-23-96; 8:45 am]
BILLING CODE 4410-09-M
