[Federal Register: August 6, 2008 (Volume 73, Number 152)]
[Notices]               
[Page 45780-45781]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06au08-85]                         

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Importer of Controlled Substances; Notice of Application

    Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to 
issuing a registration under this section to a bulk manufacturer of a 
controlled substance in schedule I or II, and prior to issuing a 
regulation under 21 U.S.C. 952(a)(2) authorizing the importation of 
such a substance, provide manufacturers holding registrations for the 
bulk manufacture of the substance an opportunity for a hearing.
    Therefore, in accordance with Title 21 Code of Federal Regulations 
(CFR), 1301.34(a), this is notice that on March 26, 2008, BA Research 
International LLC, 10550 Rockley Road, Suite 150, Houston, Texas 77099-
0000, made application to the Drug Enforcement Administration (DEA) to 
be registered as an importer of the basic classes of controlled 
substances listed in schedules I and II:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
4-Methylaminorex (cis isomer) (1590)........  I
Gamma Hydroxybutyric Acid (2010)............  I
Methaqualone (2565).........................  I
Ibogaine (7260).............................  I
Lysergic acid diethylamide (7315)...........  I
Marihuana (7360)............................  I
Tetrahydrocannabinols (7370)................  I
Cannabidiol (7372)..........................  I
Mescaline (7381)............................  I
4-Methyl-2,5-dimethoxyamphet- amine (7395)..  I
3,4-Methylenedioxyamphetamine (7400)........  I
3,4-Methylenedioxymethamphet- amine (7405)..  I
Peyote (7415)...............................  I
Bufotenine (7433)...........................  I
Diethyltryptamine (7434)....................  I
Dimethyltryptamine (7435)...................  I
Psilocybin (7437)...........................  I
Etorphine (except HCL) (9056)...............  I
Heroin (9200)...............................  I
Normorphine (9313)..........................  I
Alphacetylmethadol except levo-               I
 alphacetylmethadol (9603).
Amphetamine (1100)..........................  II
Methamphetamine (1105)......................  II
Methylphenidate (1724)......................  II
Amobarbital (2125)..........................  II
Pentobarbital (2270)........................  II
Secobarbital (2315).........................  II
Phencyclidine (7471)........................  II
Cocaine (9041)..............................  II
Codeine (9050)..............................  II
Diprenorphine (9058)........................  II
Etorphine HCL (9059)........................  II
Oxycodone (9143)............................  II
Hydromorphone (9150)........................  II
Diphenoxylate (9170)........................  II
Ethylmorphine (9190)........................  II
Levorphanol (9220)..........................  II
Dextropropoxyphene, bulk (non-dosage forms)   II
 (9273).
Thebaine (9333).............................  II
Opium, raw (9600)...........................  II
Opium, powdered (9639)......................  II
Levo-alphacetylmethadol (9648)..............  II
Oxymorphone (9652)..........................  II
Fentanyl (9801).............................  II
Hydrocodone (9193)..........................  II
Meperidine (9230)...........................  II
Methadone (9250)............................  II
Morphine (9300).............................  II
------------------------------------------------------------------------

    The company plans to import analytical reference standards for 
analytical testing of blood samples from clinical trials.
    Any bulk manufacturer who is presently, or is applying to be, 
registered with DEA to manufacture such basic classes of controlled 
substances may 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 comments or objections should be addressed, in 
quintuplicate, to the Drug Enforcement Administration, Office of 
Diversion Control, Federal Register Representative (ODL), 8701 
Morrissette Drive,

[[Page 45781]]

Springfield, Virginia 22152; and must be filed no later than September 
5, 2008.
    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), 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 30, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. E8-18045 Filed 8-5-08; 8:45 am]

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