[Federal Register: April 2, 2008 (Volume 73, Number 64)]
[Notices]
[Page 18001]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr02ap08-91]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on March 4, 2008, 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:
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Drug Schedule
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Gamma hydroxybutyric acid (2010)........... I
Amphetamine (1100)......................... II
Methylphenidate (1724)..................... II
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The company plans to manufacture bulk products for finished dosage
units and distribution to its customers.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substances, may file comments
or objections to the issuance of the proposed registration pursuant to
21 CFR Sec. 1301.33(a).
Any such written comments or objections being sent via regular mail
should be addressed, in quintuplicate, to the Drug Enforcement
Administration, Office of Diversion Control, Federal Register
Representative (ODL), Washington, DC 20537, or any being sent via
express mail should be sent to Drug Enforcement Administration, Office
of Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than June 2, 2008.
Dated: March 27, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-6775 Filed 4-1-08; 8:45 am]
BILLING CODE 4410-09-P