Notice of Application - 2012
[Federal Register Volume 77, Number 133 (Wednesday, July 11, 2012)]
[Notices]
[Page 40911]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-16918]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Importer of Controlled Substances; Notice of Application; United
States Pharmacopeial Convention
Pursuant to Title 21 Code of Federal Regulations 1301.34 (a), this
is notice that on February 17, 2012, United States Pharmacopeial
Convention, 12601 Twinbrook Parkway, Rockville, Maryland 20852, made
application by renewal to the Drug Enforcement Administration (DEA) for
registration as an importer of the following basic classes of
controlled substances:
Drug |
Schedule |
Cathinone (1235) |
I |
Methaqualone (2565) |
I |
Lysergic acid diethylamide (7315) |
I |
Marihuana (7360) |
I |
Tetrahydrocannabinols (7370) |
I |
4-Methyl-2,5-dimethoxyamphetamine (7395) |
I |
3,4-Methylenedioxyamphetamine (7400) |
I |
Codeine-N-oxide (9053) |
I |
Heroin (9200) |
I |
Morphine-N-oxide (9307) |
I |
Amphetamine (1100) |
II |
Methamphetamine (1105) |
II |
Phenmetrazine (1631) |
II |
Methylphenidate (1724) |
II |
Amobarbital (2125) |
II |
Pentobarbital (2270) |
II |
Secobarbital (2315) |
II |
Glutethimide (2550) |
II |
Phencyclidine (7471) |
II |
4-Anilino-N-phenethyl-4-piperidine (8333) |
II |
Phenylacetone (8501) |
II |
Alphaprodine (9010) |
II |
Anileridine (9020) |
II |
Cocaine (9041) |
II |
Codeine (9050) |
II |
Dihydrocodeine (9120) |
II |
Oxycodone (9143) |
II |
Hydromorphone (9150) |
II |
Diphenoxylate (9170) |
II |
Hydrocodone (9193) |
II |
Levorphanol (9220) |
II |
Meperidine (9230) |
II |
Methadone (9250) |
II |
Dextropropoxyphene, bulk (non-dosage forms) (9273) |
II |
Morphine (9300) |
II |
Thebaine (9333) |
II |
Oxymorphone (9652) |
II |
Alfentanil (9737) |
II |
Sufentanil (9740) |
II |
The company plans to import reference standards for sale to
researchers and analytical labs.
Any bulk manufacturer who is presently, or is applying to be,
registered with DEA to manufacture such basic classes of controlled
substances listed in schedule I or II, which fall under the authority
of section 1002(a)(2)(B) of the Act 21 U.S.C. 952 (a)(2)(B) may, in the
circumstances set forth in 21 U.S.C. 958(i), file comments or
objections to the issuance of the proposed registration and may, at the
same time, file a written request for a hearing on such application
pursuant to 21 CFR 1301.43, and in such form as prescribed by 21 CFR
1316.47.
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 10, 2012.
This procedure is to be conducted simultaneously with, and
independent of, the procedures described in 21 CFR 1301.34(b), (c),
(d), (e), and (f). As noted in a previous notice published in the
Federal Register on September 23, 1975, 40 FR 43745-46, all applicants
for registration to import a basic class of any controlled substance in
schedule I or II are, and will continue to be, required to demonstrate
to the Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration, that the requirements for such
registration pursuant to 21 U.S.C. 958(a); 21 U.S.C. 823(a); and 21 CFR
1301.34(b), (c), (d), (e), and (f) are satisfied.
Dated: July 2, 2012.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2012-16918 Filed 7-10-12; 8:45 am]
BILLING CODE 4410-09-P
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