[Federal Register Volume 59, Number 189 (Friday, September 30, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-24161]


[[Page Unknown]]

[Federal Register: September 30, 1994]


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DEPARTMENT OF JUSTICE
Drug Enforcement Administration

 

Manufacturer of Controlled Substances; Registration

    By Notice dated August 5, 1994, and published in the Federal 
Register on August 15, 1994, (59 FR 41785), Ciba-Geigy Corporation, 
Pharmaceutical Division, Regulatory Compliance, 556 Morris Avenue, 
Summit, New Jersey 07901, made application to the Drug Enforcement 
Administration to be registered as a bulk manufacturer of 
Methylphenidate (1724), a basic class of controlled substance listed in 
Schedule II.
    No comments or objections have been received. Therefore, pursuant 
to Section 303 of the Comprehensive Drug Abuse Prevention and Control 
Act of 1970 and Title 21, Code of Federal Regulations, Section 
1301.54(e), 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: September 22, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-24161 Filed 9-29-94; 8:45 am]
BILLING CODE 4410-09-M