[Federal Register Volume 61, Number 70 (Wednesday, April 10, 1996)]
[Notices]
[Page 15974]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-8926]



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DEPARTMENT OF JUSTICE ANTITRUST DIVISION

Manufacturer of Controlled Substances; Correction

    As set forth in the Federal Register (FR Doc. 96-4944) Vol. 61, No. 
43 at page 8303, dated March 4, 1996, Johnson Matthey, Inc., Custom 
Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey 
08066, made application to the Drug Enforcement Administration (DEA) 
for registration as a bulk manufacturer for certain controlled 
substances. The listing of controlled substances for which Johnson 
Matthey applied should have included dihydrocodeine (9120) and 
meperidine (9230).
    Any other such applicant and any person who is presently registered 
with DEA to manufacturer 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, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than June 10, 1996.

    Dated: April 3, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-8926 Filed 4-9-96; 8:45 am]
BILLING CODE 4410-09-M