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Start Preamble
Pursuant to section 1301.33(a) of title 21 of the Code of Federal Regulations (CFR), this is notice that on December 27, 1999, Organichem Corporation, 33 Riverside Avenue, Renssalaer, New York 12144, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:
Drug Schedule Methylphenidate (1724) II Meperidine (9230) II The firm plans to manufacture meperidine as bulk product for distribution to its customers and to manufacture methylphenidate for distribution to a customer.
Any other such applicant and any person who is presently registered with DEA to manufacture such substance may file comments or objections to the issuance of the proposed registration.
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 May 22, 2000.
Start SignatureMarch 13, 2000.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 00-6984 Filed 3-20-00; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 03/21/2000
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 00-6984
- Pages:
- 15178-15178 (1 pages)
- PDF File:
- 00-6984.pdf