[Federal Register: April 9, 2003 (Volume 68, Number 68)]
[Notices]
[Page 17403]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr09ap03-82]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated October 5, 2001, and published in the Federal
Register on October 17, 2001, (66 FR 52780), Boehringer Ingelheim
Chemicals, Inc., 2820 N. Normandy Drive, Petersburg, VA 23805, made
application by renewal to the Drug Enforcement Administration to be
registered as a bulk manufacturer of the basic class of controlled
substances listed below:
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Drug Schedule
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Methylphenidate (1724)..................... II
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The firm plans to manufacture the listed controlled substance for
formulation into finished pharmaceuticals.
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, Boehringer Ingelheim Chemicals,
Inc., to manufacture the listed controlled substances is consistent
with the public interest at this time. DEA has investigated Boehringer
Ingelheim Chemicals, Inc. to ensure that the company's registration is
consistent with the public interest. This 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 28 CFR 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.
Dated: March 21, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-8587 Filed 4-8-03; 8:45 am]
BILLING CODE 4410-09-M