Notice of Registration - 2012
[Federal Register Volume 77, Number 168 (Wednesday, August 29, 2012)]
[Notices]
[Page 52368]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-21282]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration;
Agilent Technologies
By Notice dated May 11, 2012, and published in the Federal Register
on May 21, 2012, 77 FR 30025, Agilent Technologies, 25200 Commercentre
Drive, Lake Forest, California 92630-8810, made application by renewal
to the Drug Enforcement Administration (DEA) to be registered as a bulk
manufacturer of the following basic classes of controlled substances:
| Drug |
Schedule |
| Phencyclidine (7471) |
II |
| 1-piperidinocyclohexanecarbonitrile (8603) |
II |
| Benzoylecgonine (9180) |
II |
The company plans to manufacture small quantities of the listed
controlled substances for use in diagnostic products.
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
Agilent Technologies to manufacture the listed basic classes of
controlled substances is consistent with the public interest at this
time. DEA has investigated Agilent Technologies 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(a), and in accordance
with 21 CFR Sec. 1301.33, the above named company is granted
registration as a bulk manufacturer of the basic classes of controlled
substances listed.
Dated: August 17, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-21282 Filed 8-28-12; 8:45 am]
BILLING CODE 4410-09-P
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