Notice of Registration - 2012
[Federal Register Volume 77, Number 246 (Friday, December 21, 2012)]
[Notices]
[Page 75671]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-30783]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration;
Euticals, Inc.
By Notice dated August 17, 2012, and published in the Federal
Register on August 29, 2012, 77 FR 52367, Euticals, Inc., (formerly
known as Archimica, Inc.), 2460 W. Bennett Street, Springfield,
Missouri 65807-1229, 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 |
| Gamma Hydroxybutyric Acid (2010) |
I |
| Amphetamine (1100) |
II |
| Lisdexamfetamine (1205) |
II |
| Methylphenidate (1724) |
II |
| Phenylacetone (8501) |
II |
| Methadone Intermediate (9254) |
II |
| Tapentadol (9780) |
II |
The company plans to manufacture the listed controlled substances
in bulk for distribution and sale to its customers.
With regards to amphetamine (1100), the company plans to acquire
the listed controlled substance in bulk from a domestic source in order
to manufacture other controlled substances in bulk for 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 Euticals, Inc., to manufacture the listed basic classes of
controlled substances is consistent with the public interest at this
time. DEA has investigated Euticals, Inc., 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 1301.33, the above named company is granted registration as a bulk
manufacturer of the basic classes of controlled substances listed.
Dated: December 14, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-30783 Filed 12-20-12; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an unofficial version. An official version of this publication may be obtained
directly from the Government Printing Office (GPO). |
