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Importers Notice of Application - 2018

[Federal Register Volume 83, Number 68 (Monday, April 9, 2018)]
[Notices]
[Pages 15175-15176]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-07167]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]

Importer of Controlled Substances Application: United States Pharmacopeial Convention

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 on or before May 9, 2018. Such persons may also file a written request for a hearing on the application on or before May 9, 2018.

ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All request for hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Attn: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY 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, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been delegated to the Assistant Administrator of the DEA Diversion Control Division ("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 March 1, 2018, United States Pharmacopeial Convention, 12601 Twinbrook Parkway, Rockville, MD, 20852 applied to be registered as an importer of the following basic classes of controlled substances:

Controlled Substance Drug Code Schedule
Cathinone 1235 I
Methaqualone 2565 I
Lysergic acid diethylamide 7315 I
4-Methyl-2,5-dimethoxyamphetamine 7395 I
4-Methoxyamphetamine 7411 I
Codeine-N-oxide 9053 I
Difenoxin 9168 I
Heroin 9200 I
Morphine-N-oxide 9307 I
Norlevorphanol 9634 I
Methamphetamine 1105 II
Phenmetrazine 1631 II
Methylphenidate 1724 II
Amobarbital 2125 II
Pentobarbital 2270 II
Secobarbital 2315 II
Glutethimide 2550 II
Phencyclidine 7471 II
Phenylacetone 8501 II
Alphaprodine 9010 II
Anileridine 9020 II
Cocaine 9041 II
Dihydrocodeine 9120 II
Diphenoxylate 9170 II
Levomethorphan 9210 II
Levorphanol 9220 II
Meperidine 9230 II
Dextropropoxyphene, bulk (non-dosage forms) 9273 II
Thebaine 9333 II
Noroxymorphone 9668 II
Alfentanil 9737 II
Sufentanil 9740 II

[[Page 15176]]

The company plans to import the bulk controlled substances for distribution of analytical reference standards to its customers for research and analytical purposes.

Dated: April 2, 2018.

Susan A. Gibson,
Deputy Assistant Administrator.

[FR Doc. 2018-07167 Filed 4-6-18; 8:45 am]

BILLING CODE 4410-09-P

 

NOTICE: This is an unofficial version. An official version of this publication may be obtained directly from the Government Printing Office (GPO).

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