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[Federal Register: July 10, 2002 (Volume 67, Number 132)]
[Notices]
[Page 45764]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr10jy02-134]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated March 27, 2002, and published in the Federal
Register on April 10, 2002, (67 FR 17468), Cody Laboratories, Inc., 331
33rd Street, Cody, Wyoming 82414, made application 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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Hydromorphone (9150)....................... II
Fentanyl (9801)............................ II
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The firms plans to bulk 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 Title 21, United States Code, section 823(a) and
determined that the registration of Cody Laboratories to manufacture
the listed controlled substances is consistent with the public interest
at this time. DEA has investigated Cody Laboratories to ensure that the
company's registration is consistent with the public interest. This
investigation 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 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: June 24, 2002.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 02-17212 Filed 7-9-02; 8:45 am]
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