[Federal Register Volume 60, Number 216 (Wednesday, November 8, 1995)]
[Notices]
[Page 56354]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-27675]



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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to section 1301.43(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on September 22, 1995, Hoffmann-
LaRoche, Inc., 340 Kingsland Street, Nutley, New Jersey 07110, made 
application to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of the Schedule II controlled 
substance levorphanol (9220).
    The firm plans to manufacture finished dosage forms for 
distribution to its customers.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substance may file comments or objections 
to the issuance of the above application.
    Any such comments or objections may be addressed to the Deputy 
Assistant Administrator, Office of Diversion Control, Drug Enforcement 
Administration, United States Department of Justice, Washington, DC 
20537, Attention: DEA Federal Register Representative (CCR), and must 
be filed no later than January 8, 1996.

    Dated: October 24, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-27675 Filed 11-7-95; 8:45 am]
BILLING CODE 4410-09-M