[Federal Register Volume 62, Number 26 (Friday, February 7, 1997)]
[Notices]
[Page 5845]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-3083]


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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated July 25, 1996, and published in the Federal 
Register on July 31, 1996, (61 FR 39986), Guilford Pharmaceuticals, 
Inc., Attn: Ross S. Laderman, 6611 Tributary Street, Baltimore, 
Maryland 21224, made application to the Drug Enforcement Administration 
(DEA) to be registered as a bulk manufacturer of cocaine (9041), a 
basic class of controlled substance listed in Schedule II.
    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. Sec. 823(a) and determined that the 
registration of Guilford Pharmaceuticals, Inc. to manufacture cocaine 
is consistent with the public interest at this time. Therefore, 
pursuant to 21 U.S.C. Sec. 823 and 28 CFR Secs. 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 class of controlled 
substance listed above is granted.

    Dated: January 9, 1997.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 97-3083 Filed 2-6-97; 8:45 am]
BILLING CODE 4410-09-M