Federal Register Notices > Notices of Registration - 2003 > Celtech Manufacturing CA, Inc. Notices of Registration - 2003FR Doc 03-768 DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances Notice of Registration By Notice dated June 10, 2002, and published in the Federal Register on June 20, 2002, (67 FR 42059), Celltech Manufacturing CA, Inc., 3501 West Garry Avenue, Santa Ana, California 92704, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of methylphenidate (1724), a basic class of controlled substance listed in Schedule II. The firm plans to manufacture the listed controlled substance to make finished dosage forms for distribution to its customers. 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 Celltech Manufacturing CA, Inc. to manufacture the listed
controlled substance is consistent with the public interest at this time.
DEA has investigated Celltech Manufacturing CA, Inc. 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 system, 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, Dated: December 13, 2002. Laura M. Nagel, [FR Doc. 03-768 Filed 1-14-03; 8:45 am]
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