[Federal Register: November 12, 2002 (Volume 67, Number 218)]
[Notices]
[Page 68686]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12no02-110]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated September 25, 2001, and published in the Federal
Register on October 3, 2001 (66 FR 50453), Cambridge Isotope Lab, 50
Frontage Road, Andover, Massachusetts 01810, 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 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
Secobarbital (2315)......................... II
Phencyclidine (7471)........................ II
Cocaine (9041).............................. II
Codeine (9050).............................. II
Oxycodone (9143)............................ II
Hydromorphone (9150)........................ II
Benzoylecgonine (9180)...................... II
Methadone (9250)............................ II
Dextropropoxyphene, bulk (non-dosage forms) II
(9273).
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 Lab to
manufacture the listed controlled substances is consistent with the
public interest at this time. DEA has investigated Cambridge Isotope
Lab on a regular basis to ensure that its continued registration is
consistent with the public interest. These investigations have included
inspection and testing of the company's physical security systems,
audits of the company's records, 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 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 above is granted.
Dated: October 21, 2002.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 02-28657 Filed 11-8-02; 8:45 am]
BILLING CODE 4410-09-M