Appendix D - 60-Day FRN

43642

Federal Register / Vol. 72, No. 150 / Monday, August 6, 2007 / Notices

a. On February 4, 2004, the President
issued Executive Order (EO) 13327,
‘‘Federal Real Property Asset
Management,’’ and established the
Federal Real Property Council (FRPC) to
oversee the Government’s asset
management planning process and to
improve governmentwide real property
performance. The EO requires the
Administrator of General Services, in
consultation with the FRPC, to develop
and maintain a centralized inventory
database, incorporating all key elements
identified by the FRPC.
b. The goals of the centralized
database are to: 1) improve decisionmaking with more accurate and reliable
data; 2) provide the ability to
benchmark Federal real property asset
performance; and 3) centralize
collection of key real property data
elements into one Federal inventory
database. The FRPP system was reengineered in FY 2005 and further
enhanced in FY 2006 to meet the
FRPC’s information technology
requirements.
c. The FY 2006 report marks the
second reporting year for the
governmentwide data elements
designated by the FRPC as required by
Executive Order 13327. All executive
branch agencies are required to submit
constructed asset-level data to the FRPP
on an annual basis. The FRPP is a
secure, password-protected Web-based
database that allows Federal real
property managers to update real
property data online and in real time,
perform historical benchmarking,
produce ad hoc reports, measure
performance of real property assets, and
identify unneeded and underutilized
assets for disposal. The FRPP Summary
Report provides information regarding
Federal real property holdings to
stakeholders.
3. How can we obtain a copy of the
FRPP summary report?

sroberts on PROD1PC70 with NOTICES

The FY 2006 version of the FRPP
Summary Report is posted on the GSA
website at http://www.gsa.gov/
realpropertyprofile. Hard copies of the
report can be obtained by contacting the
Asset Management Division (MPA),
Office of Governmentwide Policy,
General Services Administration, 1800 F
Street, N.W., Washington, DC 20405.
4. Whom should we contact for
further information regarding the FRPP?
For further information, contact
Stanley C. Langfeld, Director,
Regulations Management Division
(MPR), Office of Governmentwide
Policy, General Services

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Administration, at (202) 501–1737, or
stanley.langfeld@gsa.gov.
[FR Doc. E7–15170 Filed 8–3–07; 8:45 am]
BILLING CODE 6820–RH–S

GENERAL SERVICES
ADMINISTRATION
Federal Travel Regulation (FTR);
Maximum Per Diem Rates for the
Continental United States (CONUS)
Office of Governmentwide
Policy, General Services Administration
(GSA).
ACTION: Notice of Per Diem Bulletin 08–
01, Fiscal Year (FY) 2008 continental
United States (CONUS) per diem rates.
AGENCY:

SUMMARY: The General Services
Administration’s (GSA’s) annual per
diem review has resulted in lodging and
meal allowance rate changes for
locations within the continental United
States (CONUS) to provide for the
reimbursement of Federal employees’
authorized travel expenses covered by
per diem. Per Diem Bulletin 08–01
updates the standard CONUS lodging
per diem rate as well as the maximum
per diem amounts for existing nonstandard areas (NSAs) located within
CONUS. The standard CONUS lodging
rate will increase to $70. All CONUS per
diem rates prescribed in Bulletin 08–01
may be found at http://www.gsa.gov/
perdiem. GSA based the lodging per
diem rates, including the updated
standard CONUS lodging rate, on
average daily rate information that the
lodging industry reports. The use of
such data in the per diem rate setting
process enhances the Government’s
ability to obtain policy compliant
lodging where it is needed. In addition
to the annual lodging study, GSA
identified two new redefined nonstandard areas (NSA’s), which prompted
an out of cycle meal survey for these
areas.
For a complete listing of pertinent
information that must be submitted
through a Federal executive agency for
GSA to restudy a location if a CONUS
or standard CONUS per diem rate is
insufficient to meet necessary expenses,
please review numbers 4 and 5 of our
per diem Frequently Asked Questions at
(http://www.gsa.gov/perdiemfaqs).
DATES: This notice is effective October
1, 2007, and applies for travel
performed on or after October 1, 2007
through September 30, 2008.
FOR FURTHER INFORMATION CONTACT: For
clarification of content, contact Mr. Cy
Greenidge, Office of Governmentwide
Policy, Office of Travel, Transportation,
and Asset Management, at (202) 219–

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2349, or by e-mail at http://
www.gsa.gov/perdiemquestions. Please
cite Notice of Per Diem Bulletin 08–01.
SUPPLEMENTARY INFORMATION:
A. Background
After an analysis of current data, the
General Services Administration (GSA)
has determined that the current
standard continental United States
(CONUS) lodging rate, as well as
lodging rates for certain localities (nonstandard areas), do not adequately
reflect lodging market conditions. To
develop the per diem rates for FY 2008,
GSA used the same average daily ratebased methodology used for establishing
the FY 2007 per diem rates. The use of
average daily rate information to
establish the standard CONUS lodging
rate is new for FY 2008.
A meals study was also conducted for
two new non-standard areas (NSAs).
B. Change in Standard Procedure
GSA issues/publishes the CONUS per
diem rates, formerly published in
Appendix A to 41 CFR Chapter 301,
solely on the internet at http://
www.gsa.gov/perdiem. This process,
implemented in 2003, ensures more
timely changes in per diem rates
established by GSA for Federal
employees on official travel within
CONUS. Notices published periodically
in the Federal Register, such as this
one, now constitute the only
notification of revisions in CONUS per
diem rates to agencies.
Dated: July 31, 2007.
Becky Rhodes,
Deputy Associate Administrator.
[FR Doc. E7–15216 Filed 8–3–07; 8:45 am]
BILLING CODE 6820–14–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–07–07BO]

Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and

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Federal Register / Vol. 72, No. 150 / Monday, August 6, 2007 / Notices
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS–D74, Atlanta,
GA 30333 or send an e-mail to
omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
State of Pennsylvania Fire and Life
Safety Public Education Survey—New—

Division of Unintentional Injury,
National Center for Injury Prevention
and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).

43643

departments in Pennsylvania along with
their contact information. Fire
departments will be asked to complete
a 35-item survey either on-line or by
returning a paper survey. It is expected
that 1,000 fire departments will
complete the 30 minute survey, which
is designed to collect information on the
scope and content of educational
programs and activities, training needs,
and barriers to fire and life safety
education. An initial mailing (and email if e-mail address exists) to the fire
chief of each fire department will
include a postcard describing the study
and instructing them how to submit the
survey. Fire departments that have not
completed the survey and have not
declined will be sent a reminder
postcard and will receive a follow-up
telephone call.
There are no costs to respondents
except for their time to participate in the
surveys.

Background and Brief Description
This project will involve conducting a
statewide survey of Pennsylvania fire
departments to identify current fire and
life safety education programs,
resources, and training needs. Survey
findings will be used to develop an
inventory of programs and resources,
and to inform future training programs
for fire and life safety educators in
Pennsylvania. In the United States each
year, there are approximately 400,000
residential fires, with 14,000 non-fatal
and 3,000 fatal civilian injuries. In line
with Healthy People 2010 objectives,
National Center of Injury Prevention
and Control (NCIPC) works to reduce
and eliminate non-fatal and fatal
injuries from residential fires.
The survey will be conducted with
fire departments in Pennsylvania. The
2007 National Directory of Fire Chiefs &
EMS Administrators lists all fire

ESTIMATED ANNUALIZED BURDEN HOURS
Respondents

Number of
respondents

Number of
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
(in hours)

Fire Departments—Completed survey ............................................

1,000

1

30/60

500

............................

............................

............................

500

Total ..........................................................................................

Dated: July 31, 2007.
Marilyn S. Radke,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. E7–15218 Filed 8–3–07; 8:45 am]

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

This determination will allow FDA to
approve abbreviated new drug
applications (ANDAs) for calcium
acetate 667-mg tablet.
FOR FURTHER INFORMATION CONTACT:
Nikki Mueller, Center for Drug
Evaluation and Research (HFD–7), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–594–
2041.

Food and Drug Administration

SUPPLEMENTARY INFORMATION:

BILLING CODE 4163–18–P

[Docket Nos. 2006P–0287 and 2006P–0399]

Determination That PHOSLO (Calcium
Acetate) 667-Milligram Tablet Was Not
Withdrawn From Sale for Reasons of
Safety or Effectiveness
AGENCY:

Food and Drug Administration,

HHS.
sroberts on PROD1PC70 with NOTICES

ACTION:

Notice.

SUMMARY: The Food and Drug
Administration (FDA) has determined
that PHOSLO (calcium acetate) 667milligram (mg) tablet, equal to 169 mg
calcium, was not withdrawn from sale
for reasons of safety or effectiveness.

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In 1984,
Congress enacted the Drug Price
Competition and Patent Term
Restoration Act of 1984 (Public Law 98–
417) (the 1984 amendments), which
authorized the approval of duplicate
versions of drug products approved
under an ANDA procedure. ANDA
sponsors must, with certain exceptions,
show that the drug for which they are
seeking approval contains the same
active ingredient in the same strength
and dosage form as the ‘‘listed drug,’’
which is a version of the drug that was
previously approved. Sponsors of
ANDAs do not have to repeat the
extensive clinical testing otherwise
necessary to gain approval of a new

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drug application (NDA). The only
clinical data required in an ANDA are
data to show that the drug that is the
subject of the ANDA is bioequivalent to
the listed drug.
The 1984 amendments include what
is now section 505(j)(7) of the Federal
Food, Drug, and Cosmetic Act (21 U.S.C.
355(j)(7)), which requires FDA to
publish a list of all approved drugs.
FDA publishes this list as part of the
‘‘Approved Drug Products With
Therapeutic Equivalence Evaluations,’’
which is generally known as the
‘‘Orange Book.’’ Under FDA regulations,
drugs are withdrawn from the list if the
agency withdraws or suspends approval
of the drug’s NDA or ANDA for reasons
of safety or effectiveness or if FDA
determines that the listed drug was
withdrawn from sale for reasons of
safety or effectiveness (21 CFR 314.162).
Under § 314.161(a)(1) (21 CFR
314.161(a)(1)), the agency must
determine whether a listed drug was
withdrawn from sale for reasons of
safety or effectiveness before an ANDA
that refers to that listed drug may be
approved. FDA may not approve an

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