83 FR 39128 - Importer of Controlled Substances Registration
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 83, Issue 153 (August 8, 2018)
Drug Enforcement Administration
Federal Register Volume 83, Issue 153 (August 8, 2018)
| Page Range | 39128-39129 | |
| FR Document | 2018-16941 |
[Federal Register Volume 83, Number 153 (Wednesday, August 8, 2018)] [Notices] [Pages 39128-39129] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-16941] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Importer of Controlled Substances Registration ACTION: Notice of registration. ----------------------------------------------------------------------- SUMMARY: Registrants listed below have applied for and been granted registration by-the Drug Enforcement Administration (DEA) as importers of various classes of schedule I or II controlled substances. SUPPLEMENTARY INFORMATION: The companies listed below applied to be registered as importers of various basic classes of controlled substances. Information on previously published notices is listed in the table below. No comments or objections were submitted and no requests for hearing were submitted for these notices. [[Page 39129]] ---------------------------------------------------------------------------------------------------------------- Company FR docket Published ---------------------------------------------------------------------------------------------------------------- Restek Corporation.................................. 83 FR 27634 June 13, 2018. Bellwyck Clinical Services.......................... 83 FR 27633 June 13, 2018. Cambrex Charles City................................ 83 FR 27633 June 13, 2018. ---------------------------------------------------------------------------------------------------------------- The Drug Enforcement Administration (DEA) has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of the listed registrants to import the applicable basic classes of schedule I or II controlled substances is consistent with the public interest and with United States obligations under international treaties, conventions, or protocols in effect on May 1, 1971. The DEA investigated each company's maintenance of effective controls against diversion by inspecting and testing each company's physical security systems, verifying each company's compliance with state and local laws, and reviewing each company's background and history. Therefore, pursuant to 21 U.S.C. 952(a) and 958(a), and in accordance with 21 CFR 1301.34, the DEA has granted a registration as an importer for schedule I or II controlled substances to the above listed companies. Dated: July 31, 2018. John J. Martin, Assistant Administrator. [FR Doc. 2018-16941 Filed 8-7-18; 8:45 am] BILLING CODE 4410-09-P
![39128 Federal Register / Vol. 83, No. 153 / Wednesday, August 8, 2018 / Notices
sent to: Drug Enforcement Drug Administration, Attn: Administrator,
Controlled substance Schedule
Administration, Attn: Administrator, code 8701 Morrissette Drive, Springfield,
8701 Morrissette Drive, Springfield, Virginia 22152. All request for hearing
Marihuana ..................... 7360 I should also be sent to: (1) Drug
Virginia 22152. All request for hearing
Tetrahydrocannabinols 7370 I
should also be sent to: (1) Drug Enforcement Administration, Attn:
Enforcement Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette
The company plans to import the
Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and
listed controlled substances to
Drive, Springfield, Virginia 22152; and manufacture bulk controlled substances (2) Drug Enforcement Administration,
(2) Drug Enforcement Administration, for use in clinical trials only. Attn: DEA Federal Register
Attn: DEA Federal Register Representative/DRW, 8701 Morrissette
Dated: July 31, 2018. Drive, Springfield, Virginia 22152.
Representative/DRW, 8701 Morrissette John J. Martin,
Drive, Springfield, Virginia 22152. Comments and requests for hearings on
Assistant Administrator. applications to import narcotic raw
SUPPLEMENTARY INFORMATION: The [FR Doc. 2018–16939 Filed 8–7–18; 8:45 am] material are not appropriate. 72 FR
Attorney General has delegated his BILLING CODE 4410–09–P 3417, (January 25, 2007)
authority under the Controlled SUPPLEMENTARY INFORMATION: The
Substances Act to the Administrator of Attorney General has delegated his
the Drug Enforcement Administration DEPARTMENT OF JUSTICE
authority under the Controlled
(DEA), 28 CFR 0.100(b). Authority to Substances Act to the Administrator of
Drug Enforcement Administration
exercise all necessary functions with the Drug Enforcement Administration
respect to the promulgation and [Docket No. DEA–392] (DEA), 28 CFR 0.100(b). Authority to
implementation of 21 CFR part 1301, exercise all necessary functions with
Importer of Controlled Substances
incident to the registration of respect to the promulgation and
Application: AndersonBrecon Inc.
manufacturers, distributors, dispensers, implementation of 21 CFR part 1301,
importers, and exporters of controlled ACTION: Notice of application. incident to the registration of
substances (other than final orders in manufacturers, distributors, dispensers,
connection with suspension, denial, or DATES: Registered bulk manufacturers of importers, and exporters of controlled
revocation of registration) has been the affected basic classes, and substances (other than final orders in
redelegated to the Assistant applicants therefore, may file written connection with suspension, denial, or
Administrator of the DEA Diversion comments on or objections to the revocation of registration) has been
Control Division (‘‘Assistant issuance of the proposed registration on redelegated to the Assistant
Administrator’’) pursuant to section 7 of or before September 7, 2018. Such Administrator of the DEA Diversion
28 CFR part 0, appendix to subpart R. persons may also file a written request Control Division (‘‘Assistant
for a hearing on the application on or Administrator’’) pursuant to section 7 of
In accordance with 21 CFR before September 7, 2018. 28 CFR part 0, appendix to subpart R.
1301.34(a), this is notice that on June ADDRESSES: Written comments should In accordance with 21 CFR
29, 2018, Clinical Supplies Management be sent to: Drug Enforcement 1301.34(a), this is notice that on May 2,
Holdings, Inc., 342 42nd Street South, Administration, Attention: DEA Federal 2018, AndersonBrecon Inc., 5775
Fargo, North Dakota 58103–1132 Register Representative/DRW, 8701 Logistics Parkway, Rockford, Illinois
applied to be registered as an importer Morrissette Drive, Springfield, Virginia 61109 applied to be registered as an
of the following basic classes of 22152. All requests for hearing must be importer of the following basic class of
controlled substances: sent to: Drug Enforcement controlled substance:
Drug
Controlled substance Schedule
code
Tetrahydrocannabinols ......................................................................................................................................... 7370 I
The company plans to import the Dated: July 31, 2018. SUMMARY: Registrants listed below have
listed controlled substances for clinical John J. Martin, applied for and been granted
trial only. Approval of permit Assistant Administrator. registration by-the Drug Enforcement
applications will occur only when the [FR Doc. 2018–16937 Filed 8–7–18; 8:45 am] Administration (DEA) as importers of
registrant’s business activity is BILLING CODE 4410–09–P various classes of schedule I or II
consistent with what is authorized controlled substances.
under 21 U.S.C. 952(a)(2).
DEPARTMENT OF JUSTICE SUPPLEMENTARY INFORMATION: The
Authorization will not extend to the companies listed below applied to be
import of FDA approved or non- Drug Enforcement Administration registered as importers of various basic
approved finished dosage forms for classes of controlled substances.
[Docket No. DEA–392]
commercial sale. Information on previously published
sradovich on DSK3GMQ082PROD with NOTICES
Importer of Controlled Substances notices is listed in the table below. No
Registration comments or objections were submitted
and no requests for hearing were
ACTION: Notice of registration. submitted for these notices.
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![Federal Register / Vol. 83, No. 153 / Wednesday, August 8, 2018 / Notices 39129
Company FR docket Published
Restek Corporation ................................................................................................................... 83 FR 27634 June 13, 2018.
Bellwyck Clinical Services ........................................................................................................ 83 FR 27633 June 13, 2018.
Cambrex Charles City .............................................................................................................. 83 FR 27633 June 13, 2018.
The Drug Enforcement exercise all necessary functions with persons may also file a written request
Administration (DEA) has considered respect to the promulgation and for a hearing on the application on or
the factors in 21 U.S.C. 823, 952(a) and implementation of 21 CFR part 1301, before September 7, 2018.
958(a) and determined that the incident to the registration of ADDRESSES: Written comments should
registration of the listed registrants to manufacturers, distributors, dispensers, be sent to: Drug Enforcement
import the applicable basic classes of importers, and exporters of controlled Administration, Attention: DEA Federal
schedule I or II controlled substances is substances (other than final orders in Register Representative/DRW, 8701
consistent with the public interest and connection with suspension, denial, or Morrissette Drive, Springfield, Virginia
with United States obligations under revocation of registration) has been 22152. All requests for hearing must be
international treaties, conventions, or redelegated to the Assistant sent to: Drug Enforcement
protocols in effect on May 1, 1971. The Administrator of the DEA Diversion Administration, Attn: Administrator,
DEA investigated each company’s Control Division (‘‘Assistant 8701 Morrissette Drive, Springfield,
maintenance of effective controls Administrator’’) pursuant to section 7 of Virginia 22152. All request for hearing
against diversion by inspecting and 28 CFR part 0, appendix to subpart R. should also be sent to: (1) Drug
testing each company’s physical In accordance with 21 CFR Enforcement Administration, Attn:
security systems, verifying each 1301.33(a), this is notice that on June Hearing Clerk/LJ, 8701 Morrissette
company’s compliance with state and 25, 2018, Euticals, Inc., 2460 W Bennett Drive, Springfield, Virginia 22152; and
local laws, and reviewing each Street, Springfield, Missouri 65807– (2) Drug Enforcement Administration,
company’s background and history. 1229 applied to be registered as a bulk Attn: DEA Federal Register
Therefore, pursuant to 21 U.S.C. manufacturer of the following basic Representative/DRW, 8701 Morrissette
952(a) and 958(a), and in accordance classes of controlled substances: Drive, Springfield, Virginia 22152.
with 21 CFR 1301.34, the DEA has Comments and requests for hearings on
granted a registration as an importer for Controlled substance Drug Schedule applications to import narcotic raw
schedule I or II controlled substances to code
material are not appropriate. 72 FR
the above listed companies. 3417, (January 25, 2007)
Gamma Hydroxybutyric 2010 I
Dated: July 31, 2018. Acid. SUPPLEMENTARY INFORMATION: The
John J. Martin, Amphetamine ............... 1100 II Attorney General has delegated his
Assistant Administrator. Lisdexamfetamine ........ 1205 II authority under the Controlled
Methylphenidate ........... 1724 II Substances Act to the Administrator of
[FR Doc. 2018–16941 Filed 8–7–18; 8:45 am] Phenylacetone .............. 8501 II
BILLING CODE 4410–09–P Methadone .................... 9250 II the Drug Enforcement Administration
Methadone intermediate 9254 II (DEA), 28 CFR 0.100(b). Authority to
Oripavine ...................... 9330 II exercise all necessary functions with
DEPARTMENT OF JUSTICE Tapentadol .................... 9780 II respect to the promulgation and
implementation of 21 CFR part 1301,
Drug Enforcement Administration The company plans to manufacture incident to the registration of
[Docket No. DEA–392] the above-listed controlled substances manufacturers, distributors, dispensers,
in bulk for distribution to its customers. importers, and exporters of controlled
Bulk Manufacturer of Controlled Dated: July 31, 2018. substances (other than final orders in
Substances Application: Euticals Inc. John J. Martin, connection with suspension, denial, or
Assistant Administrator. revocation of registration) has been
ACTION: Notice of application. redelegated to the Assistant
[FR Doc. 2018–16942 Filed 8–7–18; 8:45 am]
Administrator of the DEA Diversion
DATES: Registered bulk manufacturers of BILLING CODE 4410–09–P
Control Division (‘‘Assistant
the affected basic classes, and Administrator’’) pursuant to section 7 of
applicants therefore, may file written 28 CFR part 0, appendix to subpart R.
comments on or objections to the DEPARTMENT OF JUSTICE
In accordance with 21 CFR
issuance of the proposed registration on 1301.34(a), this is notice that on August
or before October 9, 2018. Drug Enforcement Administration
16, 2017, Chattem Chemicals, Inc., 3801
ADDRESS: Written comments should be [Docket No. DEA–392] St. Elmo Avenue, Chattanooga,
sent to: Drug Enforcement Tennessee 37409 applied to be
Administration, Attention: DEA Federal Importer of Controlled Substances
registered as an importer of the
Register Representative/DRW, 8701 Application: Chattem Chemicals, Inc.
following basic classes of controlled
Morrissette Drive, Springfield, Virginia substances:
sradovich on DSK3GMQ082PROD with NOTICES
ACTION: Notice of application.
22152.
SUPPLEMENTARY INFORMATION: The DATES: Registered bulk manufacturers of Controlled Drug Schedule
the affected basic classes, and substance code
Attorney General has delegated his
authority under the Controlled applicants therefore, may file written Methamphetamine ........ 1105 II
Substances Act to the Administrator of comments on or objections to the 4-Anilino-N-phenethyl-4- 8333 II
the Drug Enforcement Administration issuance of the proposed registration on piperidine (ANPP).
(DEA), 28 CFR 0.100(b). Authority to or before September 7, 2018. Such Phenylacetone .............. 8501 II
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Document Created: 2018-08-08 02:05:31
Document Modified: 2018-08-08 02:05:31
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice of registration. | |
| FR Citation | 83 FR 39128 |
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