[Federal Register: March 11, 2004 (Volume 69, Number 48)]
[Notices]
[Page 11651-11652]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr11mr04-141]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Registration
By Notice dated November 14, 2003 and published in the Federal
Register on December 2, 2003, (68 FR 67473), Abbott Laboratories, 1776
North Centennial Drive, McPherson, Kansas 67460-1247, made application
by renewal to the Drug Enforcement Administration (DEA) to be
registered as an importer of Remifentanil (9739), a basic class of
controlled substance listed in Schedule II.
The film plans to import the remifentanil to manufacture a
controlled substance for distribution to its customers.
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 Abbott Laboratories to import the
listed controlled substance is
[[Page 11652]]
consistent with the public interest and with United States obligations
under international treaties, conventions, or protocols in effect on
May 1, 1971, at this time. DEA has investigated Abbott Laboratories on
a regular basis to ensure that the company's continued registration is
consistent with the public interest. This investigation included
inspection and testing of the company's physical security systems,
verification of the company's compliance with state and local laws, and
a review of the company's background and history. Therefore, pursuant
to section 1008(a) of the Controlled Substances Import and Export Act
and in accordance with Title 21, Code of Federal Regulations, Sec.
1301.34, the above firm is granted registration as an importer of the
basic class of controlled substance listed above.
Dated: March 3, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 04-5472 Filed 3-10-04; 8:45 am]
BILLING CODE 4410-09-M