[Federal Register: July 27, 2005 (Volume 70, Number 143)]
[Notices]
[Page 43455]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27jy05-120]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By notice dated February 23, 2005, and published in the Federal
Register on March 4, 2005 (70 FR 10680), Lin Zhi International Inc.,
687 North Pastoria Avenue, Sunnyvale, California 94085 made application
by renewal to the Drug Enforcement Administration (DEA) to be
registered as a bulk manufacturer of the basic class of controlled
substances listed in Schedule II:
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Drug Schedule
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Oxycodone (9143)........................... II
Hydrocodone (9193)......................... II
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The company plans to manufacture the listed controlled substances
in bulk for use in analysis and drug test standards.
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
Lin Zhi International Inc. to manufacture the listed basic class of
controlled substances is consistent with the public interest at this
time. DEA has investigated Lin Zhi International Inc. 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 class of controlled substances listed.
Dated: July 19, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-14828 Filed 7-26-05; 8:45 am]
BILLING CODE 4410-09-P