Notice of Application - 2010
FR Doc 2010-13752[Federal Register: June 8, 2010 (Volume 75, Number 109)]
[Notices]
[Page 32506]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr08jn10-143]
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 April 12, 2010, Boehringer
Ingelheim Chemicals Inc., 2820 N. Normandy Drive, Petersburg, Virginia
23805-9372, made application by renewal to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the
basic classes of controlled substances listed in schedule II:
| Drug |
Schedule |
| Amphetamine (1100) |
II |
| Lisdexamfetamine (1205) |
II |
| Methylphenidate (1724) |
II |
| Methadone (9250) |
II |
| Methadone Intermediate (9254) |
II |
The company plans to manufacture the listed controlled substances
in bulk for sale to its customers for formulation into finished
pharmaceuticals.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substances, 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 should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than August 9, 2010.
Dated: May 28, 2010.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2010-13752 Filed 6-7-10; 8:45 am]
BILLING CODE 4410-09-P
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