Submission for OMB Review: Comment Request, 14948-14949 [E6-4271]
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14948
Federal Register / Vol. 71, No. 57 / Friday, March 24, 2006 / Notices
Dated: February 24, 2006.
Thomas A. Readinger,
Associate Director for Offshore Minerals
Management.
[FR Doc. E6–4303 Filed 3–23–06; 8:45 am]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled
Substances; Notice of Application
BILLING CODE 4310–MR–P
Pursuant to § 1301.33(a) of Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on June 13, 2005,
Cerilliant API Services, LLC, 811
Paloma Drive, Suite A, Round Rock,
Texas 78664, made application to the
Drug Enforcement Administration
(DEA) for registration as a bulk
manufacturer of the basic classes of
controlled substances listed in Schedule
I and II; and by letter dated September
2, 2005, to modify its name to Austin
Pharma, LLC.
DEPARTMENT OF THE INTERIOR
Bureau of Reclamation
Upper Rio Grande Basin Water
Operations Review, NM; Notice of
Extension
Bureau of Reclamation,
Interior.
ACTION: Notice of extension of public
comment period for thirty days.
AGENCY:
SUMMARY: Notice is hereby given that
the comment period for the Draft
Environmental Impact Statement (DEIS)
for the Upper Rio Grande Water
Operations Review, DES–05–80, is
extended an additional 30 days to April
20, 2006.
DATES: The end of the public comment
period, as noted in the Federal Register
(71 FR 3323) on January 20, 2006, was
March 21, 2006. The public comment
period is now extended to April 20,
2006.
Written comments on the
DEIS should be addressed to Valda
Terauds, ALB–707, Bureau of
Reclamation, Albuquerque Area Office,
555 Broadway, NW., Suite 100,
Albuquerque, New Mexico 87102;
faxogram (505) 462–3593; e-mail:
vterauds@uc.usbr.gov. Our practice is to
make comments, including names and
home addresses of respondents,
available for public review. Individual
respondents may request that we
withhold their home address from
public disclosure, which we will honor
to the extent allowable by law. If you
wish us to withhold your name and/or
address, you must state this
prominently at the beginning of your
comment. We will make all submissions
from organizations or businesses, and
from individuals identifying themselves
as representatives or officials of
organizations or businesses, available
for public disclosure in their entirety.
FOR FURTHER INFORMATION CONTACT:
Valda Terauds, Resource Management
Planner, (505) 462–3584.
wwhite on PROD1PC61 with NOTICES
ADDRESSES:
Dated: March 7, 2006.
Roger Slater,
Acting Regional Director—UC Region, Bureau
of Reclamation.
[FR Doc. E6–4306 Filed 3–23–06; 8:45 am]
Drug
Schedule
Lysergic acid diethylamide (7315)
Marihuana (7360) .........................
Tetrahydrocannabinois (7370) .....
3,4–Methylenedioxyamphetamine
(7400).
3,4–Methylenedioxy-Nethylamphetamine (7404).
3,4–
Methylenedioxymethamphetamine (7405).
Psilocyn (7438) .............................
Acetyldihydrocodeine (9051) ........
Benzylmorphine (9052) ................
Codeine-N-oxide (9053) ...............
Cyprenorphine (9054) ..................
Desomorphine (9055) ...................
Etorphine (9056) ...........................
Codeine methylbromide (9070) ....
Dihydromorphine (9145) ...............
Heroin (9200) ...............................
Hydromorphinol (9301) .................
Methyldihydromorphine (9304) .....
Morphine methylbromide (9305) ..
Morphine-N-oxide (9307) .............
Alphamethadol (9605) ..................
Normethadone (9635) ..................
Amphetamine (1100) ....................
Methamphetamine (1105) ............
Cocaine (9041) .............................
Codeine (9050) .............................
Dihydrocodeine (9120) .................
Oxycodone (9143) ........................
Hydromorphone (9150) ................
Benzoylecgonine (9180) ...............
Ecgonine (9180) ...........................
Hydrocodone (9193) .....................
Levomethorphan (9210) ...............
Methadone (9250) ........................
Methadone intermediate (9254) ...
Morphine (9300) ...........................
Thebaine (9333) ...........................
Levo-alphacetylmethadol (9648) ..
Oxymorphone (9652) ...................
Poppy Straw Concentrate (9670)
Alfentanil (9737) ...........................
Remifentanil (9739) ......................
Sufentanil (9740) ..........................
Carfentanil (9743) .........................
Fentanyl (9801) ............................
BILLING CODE 4310–MN–P
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The company plans to manufacture
the listed controlled substances in bulk
for distribution to its customers.
In reference to drug code 7360
(Marihuana), the company plans to bulk
manufacture cannabidiol as a synthetic
intermediate. This controlled substance
will be further synthesized to bulk
manufacture a synthetic THC (7370). No
other activity for this drug code is
authorized for this registration.
Any other such applicant and any
person who is presently registered with
DEA to manufacture such a substance
may file comments or objections to the
issuance of the proposed registration
pursuant to 21 CFR 1301.33(a).
Any such written comments or
objections being sent via regular mail
may be addressed, in quintuplicate, to
the Deputy Assistant Administrator,
Office of Diversion Control, Drug
Enforcement Administration,
Washington, DC 20537, Attention: DEA
Federal Register Representative, Liaison
and Policy Section (ODL); or any being
sent via express mail should be sent to
DEA Headquarters, Attention: DEA
Federal Register Representative/ODL,
2401 Jefferson-Davis Highway,
Alexandria, Virginia 22301; and must be
filed no later than May 23, 2006.
Dated: March 20, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. E6–4302 Filed 3–23–06; 8:45 am]
BiLLiNG CODE 4410–09–P
DEPARTMENT OF LABOR
Office of the Secretary
Submission for OMB Review:
Comment Request
March 17, 2006.
The Department of Labor (DOL) has
submitted the following public
information collection requests (ICR) to
the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995 (Pub. L. 104–13,
44 U.S.C. chapter 35). A copy of each
ICR, with applicable supporting
documentation, may be obtained by
contacting Darrin King on 202–693–
4129 (this is not a toll-free number) or
e-mail: king.darrin@dol.gov.
Comments should be sent to Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for the
Occupational Safety and Health
Administration (OSHA), Office of
Management and Budget, Room 10235,
Washington, DC 20503, 202–395–7316
E:\FR\FM\24MRN1.SGM
24MRN1
wwhite on PROD1PC61 with NOTICES
Federal Register / Vol. 71, No. 57 / Friday, March 24, 2006 / Notices
(this is not a toll-free number), within
30 days from the date of this publication
in the Federal Register.
The OMB is particularly interested in
comments which:
• Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
• Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
• Enhance the quality, utility, and
clarity of the information to be
collected; and
• Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses.
Agency: Occupational Safety and
Health Administration.
Type of Review: Extension of
currently approved collection.
Title: Lead in General Industry (29
CFR 1910.1025).
OMB Number: 1218–0092.
Frequency: On occasion; Quarterly;
Semi-annually; and Annually.
Type of Response: Recordkeeping and
Third party disclosure.
Affected Public: Business or other forprofit; Federal Government; and State,
Local, or Tribal Government.
Number of Respondents: 62,357.
Number of Annual Responses:
4,068,503.
Estimated Time per Response: Ranges
from 1 minute to notify an employee of
their right to seek a second medical
opinion to 2 hours for an employee to
receive a medical examination.
Total Burden Hours: 1,242,562.
Total Annualized capital/startup
costs: $0.
Total Annual Costs (operating/
maintaining systems or purchasing
services): $139,869,058.
Description: The purpose of 29 CFR
1910.1025 and its information collection
requirements is to provide protection for
employees from the adverse effects
associated with occupational exposure
to the carcinogen, lead. Employers must
monitor employee exposure to lead,
provide medical surveillance, train
employees about the hazards of lead,
and establish and maintain accurate
records of employee exposure to lead.
These records are used by employers,
employees, physicians, and the
VerDate Aug<31>2005
18:26 Mar 23, 2006
Jkt 208001
Government to ensure that employees
are not being harmed by exposure to
lead.
Agency: Occupational Safety and
Health Administration.
Type of Review: Extension of
currently approved collection.
Title: Lead in Construction Standard
(29 CFR 1926.62).
OMB Number: 1218–0189.
Frequency: On occasion; Quarterly;
Semi-annually; and Annually.
Type of Response: Recordkeeping and
Third party disclosure.
Affected Public: Business or other forprofit; Federal Government; and State,
Local, or Tribal Government.
Number of Respondents: 147,073.
Number of Annual Responses:
5,782,074.
Estimated Time per Response: Ranges
from 1 minute to notify an employee of
their right to seek a second medical
opinion to 8 hours to develop a written
compliance program.
Total Burden Hours: 1,560,717.
Total Annualized capital/startup
costs: $0.
Total Annual Costs (operating/
maintaining systems or purchasing
services): $68,576,673.
Description: 29 CFR 1926.62 requires
employers to train employees about the
hazards of lead, monitor employee
exposure, to provide medical
surveillance, and maintain accurate
records of employee exposure to lead.
These records are used by employers,
employees, physicians and the
Government to ensure that employees
are not harmed by exposure to lead in
the workplace.
Ira L. Mills,
Departmental Clearance Officer.
[FR Doc. E6–4271 Filed 3–23–06; 8:45 am]
BILLING CODE 4510–26–P
DEPARTMENT OF LABOR
Office of the Secretary
Submission for OMB Review:
Comment Request
March 17, 2006.
The Department of Labor (DOL) has
submitted the following public
information collection request (ICR) to
the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995 (Pub. L. 104–
13,44 U.S.C. Chapter 35). A copy of this
ICR, with applicable supporting
documentation, may be obtained by
calling the Department of Labor. To
obtain documentation contact Ira Mills
on 202–693–4122 (this is not a toll-free
number) or e-mail: Mills.Ira@dol.gov.
PO 00000
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14949
Comments should be sent to Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for ETA, Office
of Management and Budget, Room
10235, Washington, DC 20503, 202–
395–7316 (this is not a toll free number),
within 30 days from the date of this
publication in the Federal Register.
The OMB is particularly interested in
comments which:
• Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
• Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
• Enhance the quality, utility and
clarity of the information to be
collected; and
• Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses.
Agency: Employment and Training
Administration (ETA).
Type of Review: New Collection.
Title: Generic Solicitation for Grant
Applications (SGAs).
OMB Number: 1205–0NEW.
Frequency: On occasion and annually.
Affected Public: State, Local or Tribal
Government; Business or other forprofit; Not-for-profit institutions.
Type of Response: Reporting.
Number of Respondents: 50.
Annual Responses: 5,750.
Average Response time: 20.75 hours.
Total Annual Burden Hours: 119,312.
Total Annualized Capital/Startup
Costs: $2,836,058.
Total Annual Costs (operating/
maintaining systems or purchasing
services): 0.
Description: Requesting approval for a
generic Solicitation for Grant
Application form for information
collection requirements for SGAs that
extend beyond what is collected on
currently approved standard forms.
OMB approval of this generic SGA form
will assist the Department to carry out
its responsibilities under the Paperwork
Reduction Act by accurately accounting
for the public burden associated with
grant applications through promoting a
common structure for reporting the
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Agencies
[Federal Register Volume 71, Number 57 (Friday, March 24, 2006)]
[Notices]
[Pages 14948-14949]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-4271]
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DEPARTMENT OF LABOR
Office of the Secretary
Submission for OMB Review: Comment Request
March 17, 2006.
The Department of Labor (DOL) has submitted the following public
information collection requests (ICR) to the Office of Management and
Budget (OMB) for review and approval in accordance with the Paperwork
Reduction Act of 1995 (Pub. L. 104-13, 44 U.S.C. chapter 35). A copy of
each ICR, with applicable supporting documentation, may be obtained by
contacting Darrin King on 202-693-4129 (this is not a toll-free number)
or e-mail: king.darrin@dol.gov.
Comments should be sent to Office of Information and Regulatory
Affairs, Attn: OMB Desk Officer for the Occupational Safety and Health
Administration (OSHA), Office of Management and Budget, Room 10235,
Washington, DC 20503, 202-395-7316
[[Page 14949]]
(this is not a toll-free number), within 30 days from the date of this
publication in the Federal Register.
The OMB is particularly interested in comments which:
Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
Evaluate the accuracy of the agency's estimate of the
burden of the proposed collection of information, including the
validity of the methodology and assumptions used;
Enhance the quality, utility, and clarity of the
information to be collected; and
Minimize the burden of the collection of information on
those who are to respond, including through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses.
Agency: Occupational Safety and Health Administration.
Type of Review: Extension of currently approved collection.
Title: Lead in General Industry (29 CFR 1910.1025).
OMB Number: 1218-0092.
Frequency: On occasion; Quarterly; Semi-annually; and Annually.
Type of Response: Recordkeeping and Third party disclosure.
Affected Public: Business or other for-profit; Federal Government;
and State, Local, or Tribal Government.
Number of Respondents: 62,357.
Number of Annual Responses: 4,068,503.
Estimated Time per Response: Ranges from 1 minute to notify an
employee of their right to seek a second medical opinion to 2 hours for
an employee to receive a medical examination.
Total Burden Hours: 1,242,562.
Total Annualized capital/startup costs: $0.
Total Annual Costs (operating/maintaining systems or purchasing
services): $139,869,058.
Description: The purpose of 29 CFR 1910.1025 and its information
collection requirements is to provide protection for employees from the
adverse effects associated with occupational exposure to the
carcinogen, lead. Employers must monitor employee exposure to lead,
provide medical surveillance, train employees about the hazards of
lead, and establish and maintain accurate records of employee exposure
to lead. These records are used by employers, employees, physicians,
and the Government to ensure that employees are not being harmed by
exposure to lead.
Agency: Occupational Safety and Health Administration.
Type of Review: Extension of currently approved collection.
Title: Lead in Construction Standard (29 CFR 1926.62).
OMB Number: 1218-0189.
Frequency: On occasion; Quarterly; Semi-annually; and Annually.
Type of Response: Recordkeeping and Third party disclosure.
Affected Public: Business or other for-profit; Federal Government;
and State, Local, or Tribal Government.
Number of Respondents: 147,073.
Number of Annual Responses: 5,782,074.
Estimated Time per Response: Ranges from 1 minute to notify an
employee of their right to seek a second medical opinion to 8 hours to
develop a written compliance program.
Total Burden Hours: 1,560,717.
Total Annualized capital/startup costs: $0.
Total Annual Costs (operating/maintaining systems or purchasing
services): $68,576,673.
Description: 29 CFR 1926.62 requires employers to train employees
about the hazards of lead, monitor employee exposure, to provide
medical surveillance, and maintain accurate records of employee
exposure to lead. These records are used by employers, employees,
physicians and the Government to ensure that employees are not harmed
by exposure to lead in the workplace.
Ira L. Mills,
Departmental Clearance Officer.
[FR Doc. E6-4271 Filed 3-23-06; 8:45 am]
BILLING CODE 4510-26-P