Notice of Registration - 2013
[Federal Register Volume 78, Number 17 (Friday, January 25, 2013)]
[Notices]
[Page 5503]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-01592]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances, Notice of Registration;
Morton Grove Pharmaceuticals
By Notice dated September 25, 2012, and published in the Federal
Register on October 2, 2012, 77 FR 60144, Morton Grove Pharmaceuticals,
6451 Main Street, Morton Grove, Illinois 60053-2633, made application
by letter to the Drug Enforcement Administration (DEA) to be registered
as a bulk manufacturer of Gamma Hydroxybutyric Acid (2010), a basic
class of controlled substance listed in schedule I.
The company plans to manufacture the listed controlled substance
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 Morton Grove Pharmaceuticals to manufacture the listed basic class
of controlled substance is consistent with the public interest at this
time. DEA has investigated Morton Grove Pharmaceuticals 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 class of controlled substance listed.
Dated: January 14, 2013.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2013-01592 Filed 1-24-13; 8:45 am]
BILLING CODE 4410-09-P
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