2015-09344. Importer of Controlled Substances Application: Sigma-Aldrich International GMBH, Sigma Aldrich Co., LLC
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Start Preamble
ACTION:
Notice of application.
DATES:
Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.34(a) on or before May 22, 2015. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before May 22, 2015.
ADDRESSES:
Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODXL, 8701 Morrissette Drive, Springfield, Virginia 22152. Comments and requests for hearings on applications to import narcotic raw material are not appropriate. 72 FR 3417 (January 25, 2007).
End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
The Attorney General has delegated his authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importer, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Deputy Assistant Administrator of the DEA Office of Diversion Control (“Deputy Assistant Administrator”) pursuant to section 7 of 28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR 1301.34(a), this is notice that on February 5, 2015, Sigma-Aldrich International GMBH, Sigma Aldrich Co. LLC, 3500 Dekalb Street, St. Louis, Missouri 63118 applied to be registered as an importer of the following basic classes of controlled substances:
Controlled substance Schedule Cathinone (1235) I Methcathinone (1237) I Mephedrone (4-Methyl-N-methylcathinone) (1248) I N-Ethylamphetamine (1475) I Aminorex (1585) I Gamma Hydroxybutyric Acid (2010) I Methaqualone (2565) I Alpha-ethyltryptamine (7249) I Ibogaine (7260) I Lysergic acid diethylamide (7315) I Marihuana (7360) I Tetrahydrocannabinols (7370) I Mescaline (7381) I 4-Bromo-2,5-dimethoxyamphetamine (7391) I 4-Bromo-2,5-dimethoxyphenethylamine (7392) I 4-Methyl-2,5-dimethoxyamphetamine (7395) I 2,5-Dimethoxyamphetamine (7396) I 3,4-Methylenedioxyamphetamine (7400) I N-Hydroxy-3,4-methylenedioxyamphetamine (7402) I 3,4-Methylenedioxy-N-ethylamphetamine (7404) I 3,4-Methylenedioxymethamphetamine (7405) I 4-Methoxyamphetamine (7411) I Bufotenine (7433) I Diethyltryptamine (7434) I Dimethyltryptamine (7435) I Psilocybin (7437) I Psilocyn (7438) I 1-[1-(2-Thienyl)cyclohexyl]piperidine (7470) I N-Benzylpiperazine (7493) I MDPV (3,4-Methylenedioxypyrovalerone) (7535) I Heroin (9200) I Normorphine (9313) I Etonitazene (9624) I Amphetamine (1100) II Methamphetamine (1105) II Methylphenidate (1724) II Amobarbital (2125) II Pentobarbital (2270) II Secobarbital (2315) II Glutethimide (2550) II Start Printed Page 22553 Nabilone (7379) II Phencyclidine (7471) II Cocaine (9041) II Codeine (9050) II Oxycodone (9143) II Hydromorphone (9150) II Diphenoxylate (9170) II Ecgonine (9180) II Ethylmorphine (9190) II Hydrocodone (9193) II Levorphanol (9220) II Meperidine (9230) II Methadone (9250) II Morphine (9300) II Thebaine (9333) II Opium, powdered (9639) II Levo-alphacetylmethadol (9648) II Oxymorphone (9652) II Fentanyl (9801) II The company plans to import the listed controlled substances for sale to research facilities for drug testing and analysis.
In reference to drug codes 7360 and 7370, the company plans to import a synthetic cannabidiol and a synthetic tetrahydrocannabinol. No other activity for this drug code is authorized for this registration.
Start SignatureDated: April 14, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2015-09344 Filed 4-21-15; 8:45 am]
BILLING CODE 4410-09-P
Document Information
- Published:
- 04/22/2015
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Action:
- Notice of application.
- Document Number:
- 2015-09344
- Dates:
- Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.34(a) on or before May 22, 2015. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before May 22, 2015.
- Pages:
- 22552-22553 (2 pages)
- Docket Numbers:
- Docket No. DEA-392
- PDF File:
- 2015-09344.pdf