[Federal Register Volume 64, Number 88 (Friday, May 7, 1999)]
[Notices]
[Page 24678]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-11446]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated December 2, 1998, and published in the Federal 
Register on December 11, 1998, (63 FR 68473), Cauldron Inc., DBA 
Cauldron Process Chemistry, 383 Phoenixville Pike, Malvern, 
Pennsylvania 19355, made application by renewal to the Drug Enforcement 
Administration (DEA) to be registered as a bulk manufacturer of 
amphetamine, a basic class of controlled substance listed in Schedule 
II.
    The firm plans to bulk manufacture amphetamine for the purpose of 
performing bioequivalency studies.
    DEA has considered the factors in Title 21, United States Code, 
Section 823(a) and determined that the registration of Cauldron Inc. to 
manufacture the listed controlled substance is consistent with the 
public interest at this time. DEA has investigated the firm on a 
regular basis to ensure that the company's continued registration is 
consistent with the public interest. These investigations have included 
inspection and testing of the company's physical security systems, 
audits of the company's records, verification of the company's 
compliance with state and local laws, and a review of the company's 
background and history. 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: April 26, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-11446 Filed 5-6-99; 8:45 am]
BILLING CODE 4410-09-M