Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Registration - 2000

[Federal Register: December 5, 2000 (Volume 65, Number 234)] [Notices] [Page 75957-75958] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr05de00-91]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 29, 2000, and published in the Federal Register on July 14, 2000, (65 FR 43785), 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:

Drug Schedule
Methaqualone (2565) I
Dimethyltryptamine (7435) I
Amphetamine (1100) II
Methamphetamine (1105) II
Pentobarbital (2270) II
Secobarbital (2315) II
Phencyclidine (7471) II
Phenylacetone (8501) II
Cocaine (9041) II
Codeine (9050) II
Oxycodone (9143) II
Hydromorphone (9150) II
Benzoylecgonine (9180) II
Methadone (9250) II
Dextropropoxyphene, bulk (non-dosage forms) (9273) II
Morphine (9300) II
Fentanyl (9801) II

[[Page 75958]]

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: November 20, 2000.

John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 00-30932 Filed 12-4-00; 8:45 am]

BILLING CODE 4410-09-M

 

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