Federal Register: November 16, 2007 (Volume 72, Number 221)
DOCID: fr16no07-150 FR Doc E7-22485
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
NOTICE: NOTICES
DOCID: fr16no07-150
ACTION: Applications, hearings, determinations, etc.:
SUBJECT CATEGORY:
Manufacturer of Controlled Substances; Notice of Registration
DOCUMENT SUMMARY:
By Notice dated June 26, 2007, and published in the Federal
Register on July 3, 2007, (72 FR 36483), 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 schedule I and II:
Drug Schedule Gamma hydroxybutyric acid (2010)........... I
Amphetamine (1100)......................... II
Methylphenidate (1724)..................... II
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.
Dated: November 5, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. E722485 Filed 111507; 8:45 am]
BILLING CODE 441009P
SUMMARY:
Lonza Riverside,
DOCUMENT BODY 2:
By Notice dated June 26, 2007, and published in the Federal
Register on July 3, 2007, (72 FR 36483), 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 schedule I and II:
Drug Schedule Gamma hydroxybutyric acid (2010)........... I
Amphetamine (1100)......................... II
Methylphenidate (1724)..................... II
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.
Dated: November 5, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. E722485 Filed 111507; 8:45 am]
BILLING CODE 441009P