[Federal Register Volume 61, Number 43 (Monday, March 4, 1996)]
[Notices]
[Page 8303]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-4947]
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DEPARTMENT OF JUSTICE
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated October 19, 1995, and published in the Federal
Register on October 25, 1995, (60 FR 54707), Eli Lilly Industries,
Inc., Chemical Plant, Kilometer 146 7, State Road 2, Mayaguez, Puerto
Rico 00680, made application 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 Section 303 of the
Comprehensive Drug Abuse Prevention and Control Act of 1970 and Title
21, Code of Federal Regulations, Section 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: February 26, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 96-4947 Filed 3-1-96; 8:45 am]
BILLING CODE 4410-09-M
