Importer of Controlled Substances Registration, 5500 [2019-02874]
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Federal Register / Vol. 84, No. 35 / Thursday, February 21, 2019 / Notices
Company
FR docket
Chattem Chemicals ..........................................................
83 FR 56103 ...................................................................
The DEA has considered the factors in
21 U.S.C. 823(a) and determined that
the registration of this registrant to
manufacture the applicable basic classes
of 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 the company’s maintenance
of effective controls against diversion by
inspecting and testing the company’s
physical security systems, verifying the
company’s compliance with state and
local laws, and reviewing the company’s
background and history.
Therefore, pursuant to 21 U.S.C.
823(a), and in accordance with 21 CFR
1301.33, the DEA has granted a
Dated: January 29, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019–02867 Filed 2–20–19; 8:45 am]
The registrant listed below
has applied for and been granted
registration by the Drug Enforcement
Administration (DEA) as a bulk
manufacturer of various classes of
schedule II controlled substances.
The
company listed below applied to be
registered as a bulk manufacturer of
various basic classes of controlled
substances. Information on a previously
published notice is listed below. No
comments or objections were submitted
for the notice.
SUPPLEMENTARY INFORMATION:
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Bulk Manufacturer of Controlled
Substances Registration
ACTION:
Notice of registration.
FR docket
Janssen Pharmaceuticals, Inc ..........................................
83 FR 55205 ...................................................................
registration as a bulk manufacturer to
the above listed company.
Dated: January 7, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019–02868 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–09–P
Published
November 2, 2018.
Registrants listed below have
applied for and been granted
registration by the Drug Enforcement
Administration (DEA) as importers of
schedule I or schedule II controlled
substances.
SUMMARY:
The
companies listed below applied to be
registered as importers of various basic
classes of controlled substances.
Information on the 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.
SUPPLEMENTARY INFORMATION:
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Registration
ACTION:
November 9, 2018.
SUMMARY:
Company
The DEA has considered the factors in
21 U.S.C. 823(a) and determined that
the registration of this registrant to
manufacture the applicable basic classes
of 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 the company’s maintenance
of effective controls against diversion by
inspecting and testing the company’s
physical security systems, verifying the
company’s compliance with state and
local laws, and reviewing the company’s
background and history.
Therefore, pursuant to 21 U.S.C.
823(a), and in accordance with 21 CFR
1301.33, the DEA has granted a
amozie on DSK3GDR082PROD with NOTICES1
registration as a bulk manufacturer to
the above listed company.
Published
Notice of registration.
Company
FR docket
Mylan Pharmaceuticals, Inc .........................................................................................................................
Siegfried USA, LLC ......................................................................................................................................
83 FR 64158
83 FR 64158
The 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 of the company’s
maintenance of effective controls
VerDate Sep<11>2014
17:08 Feb 20, 2019
Jkt 247001
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 registrations as importers for
schedule II controlled substances to the
above listed companies.
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Published
December 13, 2018.
December 13, 2018.
Dated: January 29, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019–02874 Filed 2–20–19; 8:45 am]
BILLING CODE 4410–09–P
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21FEN1
]]>Agencies
[Federal Register Volume 84, Number 35 (Thursday, February 21, 2019)]
[Notices]
[Page 5500]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-02874]
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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 schedule I or schedule II controlled substances.
SUPPLEMENTARY INFORMATION: The companies listed below applied to be
registered as importers of various basic classes of controlled
substances. Information on the 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.
----------------------------------------------------------------------------------------------------------------
Company FR docket Published
----------------------------------------------------------------------------------------------------------------
Mylan Pharmaceuticals, Inc............... 83 FR 64158 December 13, 2018.
Siegfried USA, LLC....................... 83 FR 64158 December 13, 2018.
----------------------------------------------------------------------------------------------------------------
The 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 of the
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 registrations as
importers for schedule II controlled substances to the above listed
companies.
Dated: January 29, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-02874 Filed 2-20-19; 8:45 am]
BILLING CODE 4410-09-P
