[Federal Register: April 29, 2009 (Volume 74, Number 81)]
[Notices]
[Page 19598]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29ap09-124]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on February 11, 2009, Siemens
Healthcare Diagnostics Inc., Attn: RA, 100 GBC Drive, Mail Stop 514,
Newark, Delaware 19702, 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 in
schedules I and II:
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Drug Schedule
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Tetrahydrocannabinols (7370)............... I
Ecgonine (9180)............................ II
Morphine (9300)............................ II
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The company plans to produce the listed controlled substances in
bulk to be used in the manufacture of reagents and drug calibrator/
controls which are DEA exempt products.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substances, may file comments
or objections to the issuance of the proposed registration pursuant to
21 CFR 1301.33(a).
Any such written comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than June 29, 2009.
Dated: April 17, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E9-9802 Filed 4-28-09; 8:45 am]
BILLING CODE 4410-09-P