[Federal Register: June 1, 2005 (Volume 70, Number 104)]
[Notices]
[Page 31539]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr01jn05-139]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated February 9, 2005, and published in the Federal
Register on February 15, 2005, (70 FR 7760), Clariant LSM (Missouri)
Inc., 2460 W. Bennett Street, Springfield, Missouri 65807-1229,
(Mailing Address: P.O. Box 1246, Springfield, Missouri 65801) made
application to the Drug Enforcement Administration (DEA) to be
registered as a bulk manufacturer of Methylphenidate (1724), a basic
class of controlled substance listed in Schedule II.
The company plans to manufacture the listed controlled substance in
bulk for research purposes.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and determined that the registration of
Clariant LSM (Missouri) Inc. to manufacture the listed basic class of
controlled substance is consistent with the public interest at this
time. DEA has investigated Clariant LSM (Missouri) Inc. to ensure that
the company's registration is consistent with the public interest. The
investigation has 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 21 U.S.C. 823, and in accordance with
21 CFR 1301.33, the above named company is granted registration as a
bulk manufacturer of the basic class of controlled substance listed.
Dated: May 25, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-10787 Filed 5-31-05; 8:45 am]
BILLING CODE 4410-09-P