[Federal Register Volume 61, Number 243 (Tuesday, December 17, 1996)]
[Notices]
[Page 66311]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-31887]


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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated September 4, 1996, and published in the Federal 
Register on September 19, 1996 (61 FR 49351), Eli Lilly Industries, 
Inc., Chemical Plant, Kilometer 146.7, State Road 2, Mayaguez, Puerto 
Rico 00680, made application for renewal to the Drug Enforcement 
Administration (DEA) for registration as a bulk manufacturer of 
dextropropoxyphene, bulk (non-dosage forms) (9273) a basic class of 
controlled substance listed in Schedule II.
    No comments or objections have been received. DEA has considered 
the factors in Title 21, United States Code, Section 823(a) and 
determined that the registration of Eli Lilly Industries, Inc. to 
manufacture the listed controlled substance is consistent with the 
public interest at this time. Therefore, pursuant to 21 U.S.C. 823 and 
28 CFR 0.100 and 0.104, 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: December 2, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-31887 Filed 12-16-96; 8:45 am]
BILLING CODE 4410-09-M