[Federal Register: March 4, 2005 (Volume 70, Number 42)]
[Notices]
[Page 10675-10676]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr04mr05-100]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances Notice of Registration
By Notice dated October 1, 2004, and published in the Federal
Register on October 29, 2004, (69 FR 63178), Cambrex North Brunswick
Inc., Technology Center of New Jersey, 661 Highway One, North
Brunswick, New Jersey 08902, 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:
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Drug Schedule
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N-Ethylamphetamine (1475).................. I
Tetrahydrocannabinols (7370)............... I
[[Page 10676]]
2,5-Dimethoxyamphetamine (7396)............ I
3,4-Methylenedioxyamphetamine (7400)....... I
4-Methoxyamphetamine (7411)................ I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Methylphenidate (1724)..................... II
Codeine (9050)............................. II
Hydromorphone (9150)....................... II
Hydrocodone (9193)......................... II
Methadone (9250)........................... II
Methadone Intermediate (9254).............. II
Morphine (9300)............................ II
Sufentanil (9740).......................... II
Fentanyl (9801)............................ II
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The company plans to manufacture the listed 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
Cambrex North Brunswick, Inc., Technology Centre of New Jersey to
manufacture the listed basic classes of controlled substances is
consistent with the public interest at this time. DEA has investigated
Cambrex North Brunswick, Inc., Technology Centre of New Jersey 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: February 23, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-4212 Filed 3-3-05; 8:45 am]
BILLING CODE 4410-09-P