Importer of Controlled Substances Application: Wildlife Laboratories, Inc., 35975 [2015-15332]
Download as PDF
<![CDATA[
Federal Register / Vol. 80, No. 120 / Tuesday, June 23, 2015 / Notices
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 January
12, 2015, Midas Pharmaceuticals, Inc.,
300 Interpace Parkway, Suite 420,
Parsippany, New Jersey 07054–1100
applied to be registered as an importer
of remifentanil (9739), a basic class of
controlled substance listed in schedule
II.
The company plans to import the
listed controlled substance in order to
bulk manufacture controlled substance
in Active Pharmaceutical Ingredient
(API) form. The company distributes the
manufactured APIs in bulk to its
customers.
Dated: June 12, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
National Archives and Records
Administration (NARA).
ACTION: Presidential Records Act notice
of proposed disposal of Reagan and
George H.W. Bush administration
disaster recovery backup tapes; final
agency action.
destruction, and a synopsis of the
completed restoration projects.
NARA has determined that the
backup tapes do not warrant further
retention. All required backup
restoration projects have taken place,
NARA is preserving and permanently
retaining the restored records, and we
have identified no further need to
preserve or maintain the backup tapes.
This notice constitutes a final agency
action, as described in 44 U.S.C.
2203(g)(3), and NARA will dispose of
the described backup tapes on or after
the date below.
DATES: NARA will dispose of the
backup tapes on or after August 24,
2015.
FOR FURTHER INFORMATION CONTACT:
Director of Presidential Libraries Susan
K. Donius, by mail at National Archives
and Records Administration, Suite
2200; 8601 Adelphi Road; College Park,
Maryland 20740–6001, by telephone at
(301) 837–3250, by fax at (301) 837–
3199, or by email at
elizabeth.fidler@nara.gov.
SUPPLEMENTARY INFORMATION: Public
comments: NARA published a
‘‘Presidential Records Act notice of
proposed disposal of Reagan and George
H.W. Bush administration disaster
recovery backup tapes; request for
public comment’’ on February 6, 2015,
in the Federal Register (80 FR 6770) for
a 45-day comment period. NARA
received one written comment, in which
a concerned citizen suggested that
NARA should retain the
‘‘documentation’’ so that it can be made
available to the public.
NARA has considered the comment.
As described in the notice of proposed
disposal, NARA is retaining the
recovered records from the backup
tapes. All the Presidential and Federal
records that were on the tapes have been
restored, and NARA is permanently
retaining those restored records. This is
in line with the commenter’s suggestion
and goal, so NARA believes no further
action is necessary in response to the
comment and is proceeding with
destruction of the backup tapes as
outlined in the proposal notice.
NARA is issuing final notice
that it intends to dispose of several
collections of disaster recovery backup
tapes from the Ronald Reagan (Reagan)
and George H.W. Bush (GHW Bush)
administrations under the provisions of
44 U.S.C. 2203(g)(3). NARA published
notice in the Federal Register (February
6, 2015 (80 FR 6770)), proposing to
dispose of these backup tapes. That
initial notice contains a detailed
description of the tapes, the reasons for
NARA action
NARA will dispose of 3,071 original
disaster recovery backup tapes created
during the Reagan and GHW Bush
administrations, and subsequent
preservation copies of those media
(maintained for the Professional/Office
Vision software (PROFS) system, the
Sperry/VAX All-in-One system, and for
systems operated by the White House
Situation Support Staff (WHSSS) and
the White House Situation Room
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
February 19, 2015, Wildlife
Laboratories, Inc., 1230 W. Ash Street,
Suite D, Windsor, Colorado 80550
applied to be registered as an importer
of the following basic classes of
controlled substances:
Controlled substance
Etorphine (except HCl) (9056) .....
Etorphine HCl (9059) ...................
[FR Doc. 2015–15331 Filed 6–22–15; 8:45 am]
Schedule
I
II
The company plans to import the
listed controlled substances for sale to
its customer.
BILLING CODE 4410–09–P
Drug Enforcement Administration
Dated: June 12, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[Docket No. DEA–392]
[FR Doc. 2015–15332 Filed 6–22–15; 8:45 am]
DEPARTMENT OF JUSTICE
BILLING CODE 4410–09–P
Importer of Controlled Substances
Application: Wildlife Laboratories, Inc.
ACTION:
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 23, 2015. Such persons
may also file a written request for a
hearing on the application pursuant to
21 CFR 1301.43 on or before July 23,
2015.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/ODXL, 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.
SUPPLEMENTARY INFORMATION: The
Attorney General has delegated his
authority under the Controlled
DATES:
mstockstill on DSK4VPTVN1PROD with NOTICES
NATIONAL ARCHIVES AND RECORDS
ADMINISTRATION
Notice of application.
VerDate Sep<11>2014
18:39 Jun 22, 2015
Jkt 235001
35975
[NARA–2015–039]
Office of Presidential Libraries;
Disposal of Presidential Records
AGENCY:
SUMMARY:
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
E:\FR\FM\23JNN1.SGM
23JNN1
]]>Agencies
[Federal Register Volume 80, Number 120 (Tuesday, June 23, 2015)]
[Notices]
[Page 35975]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-15332]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Importer of Controlled Substances Application: Wildlife
Laboratories, 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 July 23, 2015. Such persons may also file a
written request for a hearing on the application pursuant to 21 CFR
1301.43 on or before July 23, 2015.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/ODXL,
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.
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 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
February 19, 2015, Wildlife Laboratories, Inc., 1230 W. Ash Street,
Suite D, Windsor, Colorado 80550 applied to be registered as an
importer of the following basic classes of controlled substances:
------------------------------------------------------------------------
Controlled substance Schedule
------------------------------------------------------------------------
Etorphine (except HCl) (9056).............. I
Etorphine HCl (9059)....................... II
------------------------------------------------------------------------
The company plans to import the listed controlled substances for
sale to its customer.
Dated: June 12, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2015-15332 Filed 6-22-15; 8:45 am]
BILLING CODE 4410-09-P
