[Federal Register Volume 60, Number 147 (Tuesday, August 1, 1995)]
[Notices]
[Page 39186]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-18753]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Registration

    By Notice dated April 4, 1995, and published in the Federal 
Register on April 12, 1995, (60 FR 18618), 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.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-18753 Filed 7-31-95; 8:45 am]
BILLING CODE 4410-09-M