[Federal Register Volume 61, Number 230 (Wednesday, November 27, 1996)]
[Notices]
[Page 60305]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-30353]


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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 10, 1996, Hoffman-
LaRoche, Inc., 340 Kingsland Street, Nutley, New Jersey 07110, made 
application by renewal to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of levorphanol (9220) a basic class 
of controlled substance listed in Schedule II.
    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 substances may file comments or objections 
to the issuance of the above application.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than January 27, 1997.

    Dated: October 28, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-30353 Filed 11-26-96; 8:45 am]
BILLING CODE 4410-09-M