[Federal Register: April 4, 2005 (Volume 70, Number 63)]
[Notices]
[Page 17123-17124]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04ap05-131]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Importation of Controlled Substances; Notice of Application

    Pursuant to 21 U.S.C. 958(1), the Attorney General shall, prior to
issuing a registration under this Section to a bulk manufacturer of a
controlled substance in Schedule I or II and prior to issuing a
regulation under 21 U.S.C. 952(a)(2)(b) authorizing the importation of
such substances, provide manufacturers holding registrations for the
bulk manufacture of the substances an opportunity for a hearing.
    Therefore, in accordance with Title 21 CFR 1301.34(a), this is
notice that on July 26, 2004, Aveva Drug Delivery Systems Inc., 3250
Commerce Parkway, Miramar, Florida 33025-3907, made application to the
Drug Enforcement Administration (DEA) for registration as an importer
of Fentanyl (9801), a basic class of controlled substance listed in
Schedule II.
    The company plans to import the listed controlled substance for the
manufacture of analytical reference standards.
    Any manufacturer who is presently, or is applying to be, registered
with DEA to manufacture such basic classes of controlled substances may
file written 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 written comments or objections being sent via regular mail
may be addressed, in quintuplicate, to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537, Attention: DEA Federal Register
Representative, Liaison and Policy Section (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 May 4, 2004.
    This procedure is to be conducted simultaneously with and
independent of the procedures described in 21 CFR 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 43745-46), all applicants for
registration to import the basic class of any controlled substance
listed in Schedule I or II are and will continue to be required to
demonstrate to the Deputy Assistant Administrator, Office

[[Page 17124]]

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: March 25, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-6585 Filed 4-1-05; 8:45 am]

BILLING CODE 4410-09-P