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Lonza Riverside
FR Doc E8-17973[Federal Register: August 6, 2008 (Volume 73, Number 152)]
[Notices] [Page 45787-45788] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06au08-102]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated March 27, 2008, and published in the Federal Register on
April 2, 2008 (73 FR 18001), Lonza Riverside, 900 River Road, Conshohocken,
Pennsylvania 19428, made application by renewal to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the basic
classes of controlled substances listed in schedules I and II:
Drug
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Schedule
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Gamma hydroxybutyric acid (2010)
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I
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Amphetamine (1100)
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II
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Methylphenidate (1724)
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II
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The company plans to manufacture bulk products for finished dosage units and
distribution to its customers.
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 Lonza Riverside to
manufacture the listed basic classes of controlled substances is consistent with
the public interest at this time. DEA has investigated Lonza Riverside 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 classes of controlled substances listed.
[[Page 45788]]
Dated: July 28, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-17973 Filed 8-4-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
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