[Federal Register: December 2, 2003 (Volume 68, Number 231)]
[Notices]
[Page 67474-67475]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr02de03-96]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated August 19, 2003, and published in the Federal
Register on September 2, 2003, (68 FR 52224), Cambridge Isotope
Laboratories, Inc., 50 Frontage Road, Andover, Massachusetts 01810,
made application by renewal to the Drug Enforcement Administration for
registration as a bulk manufacturer of the basic classes of controlled
substances listed below:
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Drug Schedule
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Methaqualone (2565)........................ I
Dimethyltryptamine (7435................... I
Amphetamine (1100)......................... II
Methamphetamine (1105)..................... II
Pentobarbital (2270)....................... II
Secobartbital (2315)....................... II
Phencyclidine (7471)....................... II
Cocaine (9041)............................. II
Codeine (9050)............................. II
Oxycodone (9143)........................... II
Hydromorphone (9150)....................... II
Benzoylecgonine (9180)..................... II
Methadone (9250)........................... II
Dextropropoxyphene (9273).................. II
Morphine (9300)............................ II
Fentanyl (9801)............................ II
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The firm plans to manufacture small quantities of the listed
controlled substances to produce isotope labeled standards for drug
analysis.
No comments or objections have been received. DEA has considered
the factors in Title 21, United States Code, Section 823(a) and
determined that the registration of Cambridge Isotope Laboratories,
Inc. to manufacture the listed controlled substances is consistent with
the public interest at this time. DEA has investigated Cambridge
Isotope Laboratories, Inc. to ensure that the company's registration is
consistent with the public interest. this 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.
[[Page 67475]]
Therefore, pursuant to 21 U.S.C. 823 and 28 CFR 0.100 and 0.104, the
Deputy Assistant Administrator, Office of Diversion Control, hereby
orders that the application submitted by the above firm for
registration as a bulk manufacturer of the basic classes of controlled
substances listed is granted.
Dated: November 19, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-29977 Filed 12-1-03; 8:45 am]
BILLING CODE 4410-09-M