[Federal Register: February 21, 2008 (Volume 73, Number 35)]
[Notices]
[Page 9592-9593]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr21fe08-97]
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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 January 2, 2008, Siemens
Healthcare Diagnostics Inc., 100 GBC Drive, Mail Stop 514, Newark,
Delaware 19702, made application by letter 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
[[Page 9593]]
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 being sent via regular mail
should be addressed, in quintuplicate, to the Drug Enforcement
Administrator, Office of Diversion Control, Federal Register
Representative (ODL), Washington, DC 20537, or any being sent via
express mail should be sent to Drug Enforcement Administration, Office
of Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than April 21, 2008.
Dated: February 13, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-3175 Filed 2-20-08; 8:45 am]
BILLING CODE 4410-09-P