[Federal Register: May 29, 2003 (Volume 68, Number 103)]
[Notices]
[Page 32089]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29my03-148]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to section 1301.33(a) of title 21 of the Code of Federal
Regulations (CFR), this is notice that on January 28, 2003, Roche
Diagnostics Corporation, Attn: Regulatory Compliance, 9115 Hague Road,
Indianapolis, Indiana 46250, made application by renewal and on January
29, 2003, by letter to the Drug Enforcement Administration (DEA) for
registration as a bulk manufacturer of the basic classes of controlled
substances listed below:
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Drug Schedule
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Lysergic Acid Diethylamide (7315).......... I
Tetrahydrocannabinol (7370)................ I
Alphamethadol (9605)....................... I
Phencyclidine (7471)....................... II
Benzoylecogonine (9180).................... II
Methadone (9250)........................... II
Morphine (9300)............................ II
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The firm plans to manufacture small quantities of controlled
substances for use in diagnostic 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.
Any such comments or objections may be addressed, in quintuplicate,
to the Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration, United States Department of Justice,
Washington, DC 20537, Attention: Federal Register Representative,
Office of chief Counsel (CCD) and must be filed no later than July 28,
2003.
Dated: May 2, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-13313 Filed 5-28-03; 8:45 am]
BILLING CODE 4410-09-M