Airworthiness Directives; Rolls-Royce plc RB211-524 Series Turbofan Engines; Correction, 74466 [E6-21122]
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Federal Register / Vol. 71, No. 238 / Tuesday, December 12, 2006 / Rules and Regulations
part 51. Contact British Aerospace Regional
Aircraft American Support, 13850 Mclearen
Road, Herndon, Virginia 20171, for a copy of
this service information. You may review
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federal_register/code_of_federal_regulations/
ibr_locations.html.
§ 39.13
Issued in Renton, Washington, on
December 1, 2006.
Kevin M. Mullin,
Acting Manager, Transport Airplane
Directorate, Aircraft Certification Service.
[FR Doc. E6–20952 Filed 12–11–06; 8:45 am]
BILLING CODE 4910–13–P
BILLING CODE 4910–13–P
[Corrected]
On page 682, in the first column, in
the PART 39—AIRWORTHINESS
DIRECTIVES Section, in the
Applicability paragraph, in the second
line, ‘‘UL29916’’ is corrected to read
‘‘UL26916’’.
I
Issued in Burlington, Massachusetts, on
December 5, 2006.
Diane M. Cook,
Acting Manager, Engine and Propeller
Directorate, Aircraft Certification Service.
[FR Doc. E6–21122 Filed 12–11–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Part 558
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
AGENCY:
14 CFR Part 39
RIN 2120–AA64
Airworthiness Directives; Rolls-Royce
plc RB211–524 Series Turbofan
Engines; Correction
Federal Aviation
Administration, DOT.
ACTION: Final rule; correction.
AGENCY:
SUMMARY: This document makes a
correction to airworthiness directive
(AD) 2004–26–05 applicable to certain
Rolls-Royce plc (RR) RB211–524 series
turbofan engines that was published in
the Federal Register on January 5, 2005.
The part number UL29916 in the
Applicability section is incorrect. This
document corrects that part number. In
all other respects, the original document
remains the same.
DATES: Effective Date: December 12,
2006.
Ian
Dargin, Aerospace Engineer, Engine
Certification Office, FAA, Engine and
Propeller Directorate, 12 New England
Executive Park, Burlington, MA 01803–
5299; telephone (781) 238–7178; fax
(781) 238–7199.
SUPPLEMENTARY INFORMATION: A final
rule airworthiness directive FR Doc, 05–
85 applicable to RR RB211–524 series
turbofan engines, was published in the
Federal Register on January 5, 2005 (70
FR 681). The following correction is
needed:
jlentini on PROD1PC65 with RULES
FOR FURTHER INFORMATION CONTACT:
17:58 Dec 11, 2006
Food and Drug Administration,
HHS.
[Docket No. 2004–NE–19–AD; Amendment
39–13197; AD 2004–26–05]
VerDate Aug<31>2005
New Animal Drugs For Use in Animal
Feeds; Tylosin
Jkt 211001
ACTION:
Final rule.
SUMMARY: The Food and Drug
Administration (FDA) is amending the
animal drug regulations to reflect
approval of a supplemental new animal
drug application (NADA) filed by
Elanco Animal Health, A Division of Eli
Lilly & Co. The supplemental NADA
provides for an alternate feeding
regimen for tylosin phosphate in Type
C medicated swine feeds used for the
control of swine proliferative
enteropathies.
DATES: This rule is effective December
12, 2006.
FOR FURTHER INFORMATION CONTACT: Joan
C. Gotthardt, Center for Veterinary
Medicine (HFV–130), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 301–827–7571, email: joan.gotthardt@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: Elanco
Animal Health, A Division of Eli Lilly
& Co., Lilly Corporate Center,
Indianapolis, IN 46285, filed a
supplement to NADA 12–491 that
provides for use of TYLAN (tylosin
phosphate) Type A medicated articles.
The supplement provides for an
alternate feeding regimen for the control
of swine proliferative enteropathies
(ileitis) associated with Lawsonia
intracellularis. In addition, Elanco
Animal Health revised the names of
other enteric pathogens of swine to
reflect changes in the scientific
nomenclature for these bacteria. The
supplemental NADA is approved as of
November 7, 2006, and the regulations
PO 00000
Frm 00012
Fmt 4700
Sfmt 4700
in 21 CFR 558.625 are amended to
reflect the approval. The basis of
approval is discussed in the freedom of
information summary.
In accordance with the freedom of
information provisions of 21 CFR part
20 and 21 CFR 514.11(e)(2)(ii), a
summary of safety and effectiveness
data and information submitted to
support approval of this application
may be seen in the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, between 9
a.m. and 4 p.m., Monday through
Friday.
Under section 512(c)(2)(F)(iii) of the
Federal Food, Drug, and Cosmetic Act
(21 U.S.C. 360b(c)(2)(F)(iii)), this
approval qualifies for 3 years of
marketing exclusivity beginning
November 7, 2006.
FDA has determined under 21 CFR
25.33(a)(1) that this action is of a type
that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
This rule does not meet the definition
of ‘‘rule’’ in 5 U.S.C. 804(3)(A) because
it is a rule of ‘‘particular applicability.’’
Therefore, it is not subject to the
congressional review requirements in 5
U.S.C. 801–808.
List of Subjects in 21 CFR Part 558
Animal drugs, Animal feeds.
Therefore, under the Federal Food,
Drug, and Cosmetic Act and under
authority delegated to the Commissioner
of Food and Drugs and redelegated to
the Center for Veterinary Medicine, 21
CFR part 558 is amended as follows:
I
PART 558—NEW ANIMAL DRUGS FOR
USE IN ANIMAL FEEDS
1. The authority citation for 21 CFR
part 558 continues to read as follows:
I
Authority: 21 U.S.C. 360b, 371.
2. In § 558.625, revise paragraphs
(f)(1)(i)(b), (f)(1)(vi)(b)(1), (f)(1)(vi)(c)(1),
and (f)(1)(vi)(e)(1) to read as follows:
I
§ 558.625
Tylosin.
*
*
*
*
*
(f) * * *
(1) * * *
(i) * * *
(b) Indications for use. For reduction
of incidence of liver abscesses caused by
Fusobacterium necrophorum and
Arcanobacterium (Actinomyces)
pyogenes.
*
*
*
*
*
(vi) * * *
E:\FR\FM\12DER1.SGM
12DER1
Agencies
[Federal Register Volume 71, Number 238 (Tuesday, December 12, 2006)]
[Rules and Regulations]
[Page 74466]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-21122]
-----------------------------------------------------------------------
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 39
[Docket No. 2004-NE-19-AD; Amendment 39-13197; AD 2004-26-05]
RIN 2120-AA64
Airworthiness Directives; Rolls-Royce plc RB211-524 Series
Turbofan Engines; Correction
AGENCY: Federal Aviation Administration, DOT.
ACTION: Final rule; correction.
-----------------------------------------------------------------------
SUMMARY: This document makes a correction to airworthiness directive
(AD) 2004-26-05 applicable to certain Rolls-Royce plc (RR) RB211-524
series turbofan engines that was published in the Federal Register on
January 5, 2005. The part number UL29916 in the Applicability section
is incorrect. This document corrects that part number. In all other
respects, the original document remains the same.
DATES: Effective Date: December 12, 2006.
FOR FURTHER INFORMATION CONTACT: Ian Dargin, Aerospace Engineer, Engine
Certification Office, FAA, Engine and Propeller Directorate, 12 New
England Executive Park, Burlington, MA 01803-5299; telephone (781) 238-
7178; fax (781) 238-7199.
SUPPLEMENTARY INFORMATION: A final rule airworthiness directive FR Doc,
05-85 applicable to RR RB211-524 series turbofan engines, was published
in the Federal Register on January 5, 2005 (70 FR 681). The following
correction is needed:
Sec. 39.13 [Corrected]
0
On page 682, in the first column, in the PART 39--AIRWORTHINESS
DIRECTIVES Section, in the Applicability paragraph, in the second line,
``UL29916'' is corrected to read ``UL26916''.
Issued in Burlington, Massachusetts, on December 5, 2006.
Diane M. Cook,
Acting Manager, Engine and Propeller Directorate, Aircraft
Certification Service.
[FR Doc. E6-21122 Filed 12-11-06; 8:45 am]
BILLING CODE 4910-13-P