Importer of Controlled Substances Application: Cerilliant Corporation, 25335 [2017-11387]
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25335
Federal Register / Vol. 82, No. 104 / Thursday, June 1, 2017 / Notices
Dated: May 23, 2017.
Louis J. Milione,
Assistant Administrator.
The company plans to manufacture
small quantities of the listed controlled
substance in bulk for distribution to its
customers.
[FR Doc. 2017–11383 Filed 5–31–17; 8:45 am]
Dated: May 23, 2017.
Louis J. Milione,
Assistant Administrator.
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
[FR Doc. 2017–11385 Filed 5–31–17; 8:45 am]
BILLING CODE 4410–09–P
Drug Enforcement Administration
[Docket No. DEA–392]
DEPARTMENT OF JUSTICE
Bulk Manufacturer of Controlled
Substances Application: Chemtos,
LLC
ACTION:
Drug Enforcement Administration
[Docket No. DEA–392]
Notice of application.
Registered bulk manufacturers of
the affected basic class, and applicants
therefore, may file written comments on
or objections to the issuance of the
proposed registration in accordance
with 21 CFR 1301.33(a) on or before July
31, 2017.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DRW 8701
Morrissette Drive, Springfield, Virginia
22152.
DATES:
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
redelegated 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
1301.33(a), this is notice that on July 5,
2016, Chemtos, LLC, 14101 W. Highway
290, Building 2000B, Austin, Texas
78737–9331 applied to be registered as
a bulk manufacturer for 3,4Methylenedioxymethamphetamine
(7405), a basic class of controlled
substance listed in schedule I.
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SUPPLEMENTARY INFORMATION:
Importer of Controlled Substances
Application: Cerilliant Corporation
ACTION:
Notice of application.
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 July 3, 2017]. Such persons
may also file a written request for a
hearing on the application pursuant to
21 CFR 1301.43 on or before July 3,
2017.
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 requests 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
DATES:
manufacturers, distributors, dispensers,
importers, and exporters of controlled
substances (other than final orders in
connection with suspension, denial, or
revocation of registration) has been
redelegated 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 April
6, 2017, Cerilliant Corporation, 811
Paloma Drive, Suite A, Round Rock,
Texas 78665–2402 applied to be
registered as an importer of U–47700
(3,4-dichloro-N-[2dimethylamino)cyclohexyl]-Nmethylbenzamide) (9547), a basic class
of controlled substance listed in
schedule I.
The company plans to import small
quantities of the listed controlled
substance for the manufacture of
analytical reference standards and
distribution to their research and
forensic customers.
Dated: May 25, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017–11387 Filed 5–31–17; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Registration
ACTION:
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.
SUMMARY:
Company
FR docket
Chattem Chemicals, Inc .................................................................................................................................
Anderson Brecon, Inc ....................................................................................................................................
Hospira ...........................................................................................................................................................
Myoderm ........................................................................................................................................................
Meridian Medical Technologies .....................................................................................................................
VerDate Sep<11>2014
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Published
September 8, 2016.
October 18, 2016.
February 21, 2017.
March 9, 2017.
March 9, 2017.
Agencies
[Federal Register Volume 82, Number 104 (Thursday, June 1, 2017)]
[Notices]
[Page 25335]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-11387]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Importer of Controlled Substances Application: Cerilliant
Corporation
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 July 3, 2017]. Such persons may also file a
written request for a hearing on the application pursuant to 21 CFR
1301.43 on or before July 3, 2017.
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
requests 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 redelegated
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 April
6, 2017, Cerilliant Corporation, 811 Paloma Drive, Suite A, Round Rock,
Texas 78665-2402 applied to be registered as an importer of U-47700
(3,4-dichloro-N-[2-dimethylamino)cyclohexyl]-N-methylbenzamide) (9547),
a basic class of controlled substance listed in schedule I.
The company plans to import small quantities of the listed
controlled substance for the manufacture of analytical reference
standards and distribution to their research and forensic customers.
Dated: May 25, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017-11387 Filed 5-31-17; 8:45 am]
BILLING CODE 4410-09-P