[Federal Register: June 20, 2007 (Volume 72, Number 118)]
[Notices]
[Page 34040]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr20jn07-132]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Application
Pursuant to Title 21 Code of Federal Regulations 1301.34(a), this
is notice that on April 23, 2007, Cambrex Charles City, Inc., 1205 11th
Street, Charles City, Iowa 50616-3466, made application by letter to
the Drug Enforcement Administration (DEA) for registration as an
importer of the basic classes of controlled substances listed in
schedules II:
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Drug Schedule
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Thebaine (9333)............................ II
Raw Opium (9600)........................... II
Concentrate of Poppy Straw (9670).......... II
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The company plans to import the listed controlled substances for
manufacture of active pharmaceutical ingredients for sale to its
customers.
No comments, objections, or requests for any hearings will be
received on any application for registration or re-registration to
import crude opium, poppy straw, concentrate of poppy straw, and coca
leaves.
Any bulk manufacturer who is presently, or is applying to be,
registered with DEA to manufacture such basic classes of controlled
substances listed in schedule I or II, which fall under the authority
of section 1002(a)(2)(B) of the Act (21 U.S.C. 952(a)(2)(B)) may file
comments or objections to the issuance of the proposed registration and
may, at the same time, file a written request for a hearing on such
application pursuant to 21 CFR 1301.43 and in such form as prescribed
by 21 CFR 1316.47.
Any such comments or objections may be addressed, in quintuplicate,
to the Drug Enforcement Administration, Office of Diversion Control,
Federal Register Representative (ODL), Washington, DC 20537; or any
being sent via express mail should be sent to Drug Enforcement
Administration, Office of Diversion Control, Federal Register
Representative (ODL), 2401 Jefferson-Davis Highway, Alexandria,
Virginia 22301; and must be filed no later than July 20, 2007.
This procedure is to be conducted simultaneously with and
independent of the procedures described in 21 CFR Sec. 1301.34(b),
(c), (d), (e) and (f). As noted in a previous notice published in the
Federal Register on September 23, 1975, (40 FR 43745), all applicants
for registration to import a basic class of any controlled substances
in schedule I or II are and will continue to be required to demonstrate
to the Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration, that the requirements for such
registration pursuant to 21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR
1301.34(b), (c), (d), (e) and (f) are satisfied.
Dated: June 7, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E7-11915 Filed 6-19-07; 8:45 am]
BILLING CODE 4410-09-P