Manufacturer of Controlled Substances; Notice of Registration, 9967 [E7-3919]
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9967
Federal Register / Vol. 72, No. 43 / Tuesday, March 6, 2007 / Notices
Title: Certification Summary Form,
Reporting Summary Form for Acreage
Limitation, 43 CFR part 426 and 43 CFR
part 428.
Abstract: These forms are to be used
by district offices to summarize
individual landholder (direct or indirect
landowner or lessee) and farm operator
certification and reporting forms as
required by the RRA, 43 CFR part 426,
and 43 CFR part 428. This information
allows us to establish water user
compliance with Federal reclamation
law.
Changes to the RRA forms and the
instructions to those forms. The changes
made to the current Form 7–21SUMM–
C, Form 7–21SUMM–R, and the
corresponding instructions clarify the
completion instructions for these forms
(for example, adding verbiage to clarify
when requested acreages are to be
provided on a westwide or districtspecific basis). Other changes to the
forms and the corresponding
instructions are editorial in nature and
are designed to assist the respondents
by increasing their understanding of the
forms, and clarifying the instructions for
use when completing the forms. The
Burden estimate per form
(in hours)
Form No.
proposed revisions to the RRA forms
will be effective in the 2008 water year.
Frequency: Annually.
Respondents: Contracting entities that
are subject to the acreage limitation
provisions of Federal reclamation law.
Estimated Total Number of
Respondents: 225.
Estimated Number of Responses per
Respondent: 1.25.
Estimated Total Number of Annual
Responses: 281.
Estimated Total Annual Burden on
Respondents: 11,240 hours.
Estimate of Burden for Each Form:
Number of
respondents
Annual number of
responses
Annual burden
on respondents
(in hours)
7–21SUMM–C and associated tabulation sheets ...........................................
7–21SUMM–R and associated tabulation sheets ...........................................
40
40
188
37
235
46
9,400
1,840
Totals ........................................................................................................
........................
225
281
11,240
cprice-sewell on PROD1PC67 with NOTICES
Comments
Comments are invited on:
(a) Whether the proposed collection of
information is necessary for the proper
performance of our functions, including
whether the information will have
practical use;
(b) The accuracy of our burden
estimate for the proposed collection of
information;
(c) Ways to enhance the quality,
usefulness, and clarity of the
information to be collected; and
(d) Ways to minimize the burden of
the collection of information on
respondents, including the use of
automated collection techniques or
other forms of information technology.
We will summarize all comments
received regarding this notice. We will
publish that summary in the Federal
Register when the information
collection request is submitted to OMB
for review and approval.
Before including your address,
telephone number, e-mail address, or
other personal identifying information
in your comment, you should be aware
that your entire comment—including
your personal identifying information—
may be made publicly available at any
time. While you can ask us in your
comment to withhold your personal
identifying information from public
review, we cannot guarantee that we
will be able to do so.
VerDate Aug<31>2005
15:35 Mar 05, 2007
Jkt 211001
Dated: January 29, 2007.
Roseann Gonzales,
Director, Office of Program and Policy
Services, Denver Office.
[FR Doc. E7–3847 Filed 3–5–07; 8:45 am]
BILLING CODE 4310–MN–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Registration
By Notice dated October 11, 2006, and
published in the Federal Register on
October 18, 2006, (71 FR 61511), Varian,
Inc., Lake Forest, 25200 Commercentre
Drive, Lake Forest, California 92630–
8810, made application by renewal to
the Drug Enforcement Administration
(DEA) to be registered as a bulk
manufacturer of the basic classes of
controlled substances listed in schedule
II:
Drug
II
II
II
The company plans to manufacture
small quantities of the listed controlled
substances for use in diagnostic
products.
No comments or objections have been
received. DEA has considered the
factors in 21 U.S.C. 823(a) and
determined that the registration of
Varian, Inc., Lake Forest to manufacture
Frm 00050
Fmt 4703
Dated: February 26, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. E7–3919 Filed 3–5–07; 8:45 am]
BILLING CODE 4410–09–P
Schedule
Phencyclidine (7471) ....................
1–Piperidinocyclohexanecarbonitrile (8603)
Benzoylecgonine (9180) ...............
PO 00000
the listed basic classes of controlled
substances is consistent with the public
interest at this time. DEA has
investigated Varian, Inc., Lake Forest to
ensure that the company’s registration is
consistent with the public interest. The
investigation has included inspection
and testing of the company’s physical
security systems, verification of the
company’s compliance with state and
local laws, and a review of the
company’s background and history.
Therefore, pursuant to 21 U.S.C. 823,
and in accordance with 21 CFR 1301.33,
the above named company is granted
registration as a bulk manufacturer of
the basic classes of controlled
substances listed.
Sfmt 4703
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
ATF Fitness Products, Inc.; Denial of
Application
On February 6, 2006, the Deputy
Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration, issued an Order to
Show Cause to ATF Fitness Products,
Inc. (Respondent) of Oakmont, Pa. The
Show Cause Order proposed to deny
Respondent’s pending application for
E:\FR\FM\06MRN1.SGM
06MRN1
]]>Agencies
[Federal Register Volume 72, Number 43 (Tuesday, March 6, 2007)]
[Notices]
[Page 9967]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-3919]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated October 11, 2006, and published in the Federal
Register on October 18, 2006, (71 FR 61511), Varian, Inc., Lake Forest,
25200 Commercentre Drive, Lake Forest, California 92630-8810, made
application by renewal to the Drug Enforcement Administration (DEA) to
be registered as a bulk manufacturer of the basic classes of controlled
substances listed in schedule II:
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Phencyclidine (7471)....................... II
1-Piperidinocyclohexane-carbonitrile (8603) II
Benzoylecgonine (9180)..................... II
------------------------------------------------------------------------
The company plans to manufacture small quantities of the listed
controlled substances for use in diagnostic products.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and determined that the registration of
Varian, Inc., Lake Forest to manufacture the listed basic classes of
controlled substances is consistent with the public interest at this
time. DEA has investigated Varian, Inc., Lake Forest to ensure that the
company's registration is consistent with the public interest. The
investigation has included inspection and testing of the company's
physical security systems, verification of the company's compliance
with state and local laws, and a review of the company's background and
history. Therefore, pursuant to 21 U.S.C. 823, and in accordance with
21 CFR 1301.33, the above named company is granted registration as a
bulk manufacturer of the basic classes of controlled substances listed.
Dated: February 26, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E7-3919 Filed 3-5-07; 8:45 am]
BILLING CODE 4410-09-P
