[Federal Register Volume 59, Number 230 (Thursday, December 1, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-29526]


[[Page Unknown]]

[Federal Register: December 1, 1994]


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DEPARTMENT OF JUSTICE
Drug Enforcement Administration

 

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated September 28, 1994, and published in the Federal 
Register on October 5, 1994, (59 FR 50773), Knoll Pharmaceuticals, 30 
North Jefferson Road, Whippany, New Jersey 07981, made application to 
the Drug Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of Hydromorphone (9150), 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, Sec. 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: November 22, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-29526 Filed 11-30-94; 8:45 am]
BILLING CODE 4410-09-M