Importer of Controlled Substances Application: Johnson Matthey, Inc., 81367 [2015-32640]
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Federal Register / Vol. 80, No. 249 / Tuesday, December 29, 2015 / Notices
continuing or entering into agreements
in a form customarily used in the
industry to (1) share news helicopters or
(2) pool generic video footage that does
not include recording a reporter or other
on-air talent, and does not preclude
Defendants from entering into any nonsales-related shared services agreement
or transition services agreement that is
approved in advance by the United
States in its sole discretion.
XII. RETENTION OF JURISDICTION
This Court retains jurisdiction to
enable any party to this Final Judgment
to apply to this Court at any time for
further orders and directions as may be
necessary or appropriate to carry out or
construe this Final Judgment, to modify
any of its provisions, to enforce
compliance, and to punish violations of
its provisions.
comments on or objections to the
issuance of the proposed registration in
accordance with 21 CFR 1301.34(a) on
or before January 28, 2016.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/ODW, 8701
Morrissette Drive, Springfield, Virginia
22152. Request for hearings should be
sent to: Drug Enforcement
Administration, Attention: Hearing
Clerk/LJ, 8701 Morrissette Drive,
Springfield, Virginia 22152. Comments
and request for hearings on applications
to import narcotic raw material are not
appropriate. 72 FR 3417, (January 25,
2007).
The
Attorney General has delegated her
authority under the Controlled
Substances Act to the Administrator of
XIII. EXPIRATION OF FINAL
the Drug Enforcement Administration
JUDGMENT
(DEA), 28 CFR 0.100(b). Authority to
Unless this Court grants an extension, exercise all necessary functions with
this Final Judgment shall expire ten
respect to the promulgation and
years from the date of its entry.
implementation of 21 CFR part 1301,
incident to the registration of
XIV. PUBLIC INTEREST
manufacturers, distributors, dispensers,
DETERMINATION
importers, and exporters of controlled
Entry of this Final Judgment is in the
substances (other than final orders in
public interest. The parties have
connection with suspension, denial, or
complied with the requirements of the
revocation of registration) has been
Antitrust Procedures and Penalties Act,
redelegated to the Deputy Assistant
15 U.S.C. 16, including making copies
Administrator of the DEA Office of
available to the public of this Final
Diversion Control (‘‘Deputy Assistant
Judgment, the Competitive Impact
Administrator’’) pursuant to section 7 of
Statement, and any comments thereon,
28 CFR part 0, appendix to subpart R.
and the United States’ responses to
In accordance with 21 CFR
comments. Based upon the record
1301.34(a), this is notice that on
before the Court, which includes the
September 3, 2015, Johnson Matthey,
Competitive Impact Statement and any
Inc., Pharmaceutical Materials, 2003
comments and response to comments
Nolte Drive, West Deptford, New Jersey
filed with the Court, entry of this Final
08066–1742 applied to be registered as
Judgment is in the public interest.
an importer of the following basic
Date: llllllllllllllllll classes of controlled substances:
Court approval subject to procedures of
Antitrust Procedures and Penalties Act, 15
U.S.C. 16
lllllllllllllllllllll
United States District Judge
[FR Doc. 2015–32785 Filed 12–28–15; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Application: Johnson Matthey, Inc.
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic classes, and
applicants therefore, may file written
DATES:
VerDate Sep<11>2014
19:17 Dec 28, 2015
Jkt 238001
SUPPLEMENTARY INFORMATION:
Controlled substance
Coca Leaves (9040) .....................
Thebaine (9333) ...........................
Opium, raw (9600) .......................
Noroxymorphone (9668) ..............
Poppy Straw Concentrate (9670)
Fentanyl (9801) ............................
Schedule
II
II
II
II
II
II
The company plans to import
thebaine derivatives and fentanyl as
reference standards.
The company plans to import the
remaining listed controlled substances
as raw materials, to be used in the
manufacture of bulk controlled
substances, for distribution to its
customers. Placement of these drug
codes onto the company’s registration
does not translate into automatic
approval of subsequent permit
PO 00000
Frm 00096
Fmt 4703
Sfmt 4703
81367
applications to import controlled
substances.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C, 952(a)(2).
Authorization will not extend to the
import of FDA approved or nonapproved finished dosage forms for
commercial sale.
Dated: December 21, 2015.
Louis J. Milione,
Deputy Assistant Administrator.
[FR Doc. 2015–32640 Filed 12–28–15; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Notice of Lodging of Proposed
Consent Decree Under the
Comprehensive Environmental
Response, Compensation, and Liability
Act
On December 21, 2015, the
Department of Justice lodged a proposed
Consent Decree with the United States
District Court for the Northern District
of Indiana in the lawsuit entitled United
States and the State of Indiana v.
Anderson Products Inc., et al, Civil
Action No. 15–613.
The United States and the State filed
the lawsuit under the Comprehensive
Environmental Response,
Compensation, and Liability Act
(CERCLA). The Complaint names seven
parties as Defendants: Anderson
Products Inc., doing business in Indiana
as Anco Products, Inc.; B–D Industries;
Elkhart Plating Corp.; FFP Holdings,
LLC, formerly known as Flexible Foam
Products, Inc.; Gaska Tape Inc.; Holland
Metal Fab, Inc.; and Walerko Tool and
Engineering Corp. The Complaint seeks
recovery of certain costs that the United
States and the State incurred and/or will
incur in responding to releases of
hazardous substances at the Lusher
Street Groundwater Contamination
Superfund Site located in the City of
Elkhart, Elkhart County, Indiana. This
includes the State’s past costs of
$26,436.38. The Consent Decree
requires Defendants to reimburse those
State costs and perform injunctive relief
related to groundwater contamination
and associated soil vapor for Operable
Unit 1 at the Site. In return, the United
States and the State agree not to pursue
the Defendants under Sections 106 and
107 of CERCLA for the matters
addressed in the Consent Decree.
The publication of this notice opens
a period for public comment on the
proposed Consent Decree. Comments
should be addressed to the Assistant
Attorney General, Environment and
E:\FR\FM\29DEN1.SGM
29DEN1
]]>Agencies
[Federal Register Volume 80, Number 249 (Tuesday, December 29, 2015)]
[Notices]
[Page 81367]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-32640]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Importer of Controlled Substances Application: Johnson Matthey,
Inc.
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 January 28, 2016.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/ODW,
8701 Morrissette Drive, Springfield, Virginia 22152. Request for
hearings should be sent to: Drug Enforcement Administration, Attention:
Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152.
Comments and request for hearings on applications to import narcotic
raw material are not appropriate. 72 FR 3417, (January 25, 2007).
SUPPLEMENTARY INFORMATION: The Attorney General has delegated her
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 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
September 3, 2015, Johnson Matthey, Inc., Pharmaceutical Materials,
2003 Nolte Drive, West Deptford, New Jersey 08066-1742 applied to be
registered as an importer of the following basic classes of controlled
substances:
------------------------------------------------------------------------
Controlled substance Schedule
------------------------------------------------------------------------
Coca Leaves (9040)......................... II
Thebaine (9333)............................ II
Opium, raw (9600).......................... II
Noroxymorphone (9668)...................... II
Poppy Straw Concentrate (9670)............. II
Fentanyl (9801)............................ II
------------------------------------------------------------------------
The company plans to import thebaine derivatives and fentanyl as
reference standards.
The company plans to import the remaining listed controlled
substances as raw materials, to be used in the manufacture of bulk
controlled substances, for distribution to its customers. Placement of
these drug codes onto the company's registration does not translate
into automatic approval of subsequent permit applications to import
controlled substances.
Approval of permit applications will occur only when the
registrant's business activity is consistent with what is authorized
under 21 U.S.C, 952(a)(2). Authorization will not extend to the import
of FDA approved or non-approved finished dosage forms for commercial
sale.
Dated: December 21, 2015.
Louis J. Milione,
Deputy Assistant Administrator.
[FR Doc. 2015-32640 Filed 12-28-15; 8:45 am]
BILLING CODE 4410-09-P
