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Johnson Matthey, Inc
FR Doc E8-6379[Federal Register: March 28, 2008 (Volume 73, Number 61)]
[Notices] [Page 16711] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr28mr08-110]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated December 17, 2007, and published in the Federal Register on
December 27, 2007, (72 FR 73359), Johnson Matthey, Inc., Custom Pharmaceuticals
Department, 2003 Nolte Drive, West Deptford, New Jersey 08066-1742, 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 schedules I and II:
Drug
|
Schedule
|
Tetrahydrocannabinols (7370)
|
I
|
Dihydromorphine (9145)
|
I
|
Difenoxin (9168)
|
I
|
Propiram (9649)
|
I
|
Amphetamine (1100)
|
II
|
Methamphetamine (1105)
|
II
|
Methylphenidate (1724)
|
II
|
Nabilone (7379)
|
II
|
Cocaine (9041)
|
II
|
Codeine (9050)
|
II
|
Dihydrocodeine (9120)
|
II
|
Oxycodone (9143)
|
II
|
Hydromorphone (9150)
|
II
|
Ecgonine (9180)
|
II
|
Hydrocodone (9193)
|
II
|
Meperidine (9230)
|
II
|
Methadone (9250)
|
II
|
Methadone intermediate (9254)
|
II
|
Morphine (9300)
|
II
|
Thebaine (9333)
|
II
|
Oxymorphone (9652)
|
II
|
Noroxymorphone (9668)
|
II
|
Alfentanil (9737)
|
II
|
Remifentanil (9739)
|
II
|
Sufentanil (9740)
|
II
|
Fentanyl (9801)
|
II
|
The company plans to manufacture the listed controlled substances in bulk for
sale 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 Johnson Matthey,
Inc. to manufacture the listed basic classes of controlled substances is
consistent with the public interest at this time. DEA has investigated Johnson
Matthey, 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, 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: March 19, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration.
[FR Doc. E8-6379 Filed 3-27-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
directly from the Government Printing Office (GPO).
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