Notice of Application - 2011
[Federal Register Volume 76, Number 229 (Tuesday, November 29, 2011)]
[Notices]
[Page 73679]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-30689]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal
Regulations (CFR), this is notice that on August 9, 2011, Johnson
Matthey, Inc., Pharmaceuticals Materials, 900 River Road, Conshohocken,
Pennsylvania 19428, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the
following basic classes of controlled substances:
| Drug |
Schedule |
| Diphenoxylate (9170) |
II |
| Meperidine (9230) |
II |
| Methadone (9250) |
II |
| Methadone Intermediate (9254) |
II |
The company plans to manufacture the listed controlled substances
in bulk for distribution and sale 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 1301.33(a).
Any such written comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than January 30, 2012.
Dated: November 21, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-30689 Filed 11-28-11; 8:45 am]
BILLING CODE 4410-09-P
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