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Johnson Matthey, Inc.
FR Doc E8-3176 [Federal Register: February 21, 2008 (Volume 73, Number 35)]
[Notices] [Page 9592] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr21fe08-96]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR),
this is notice that on December 10, 2007, Johnson Matthey, Inc., Custom
Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey
08066-1742, made application by letter to the Drug Enforcement Administration (DEA)
to be registered as a bulk manufacturer of Lisdexamfetamine (1205), a basic
class of controlled substance listed in schedule II.
The company plans to manufacture the listed controlled substance in bulk for
sale to its customers. 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 pursuant to 21
CFR 1301.33(a).
Any such written comments or objections being sent via regular mail should be
addressed, in quintuplicate, to the Drug Enforcement Administrator, Office of
Diversion Control, Federal Register Representative (ODL), Washington, DC 20537,
or any being sent via express mail should be sent to Drug Enforcement
Administration, Office of Diversion Control, Federal Register Representative (ODL),
8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later
than April 21, 2008.
Dated: February 13, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-3176 Filed 2-20-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
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