Human Space Flight Requirements for Crew and Space Flight Participants, 27732-27733 [E7-9480]

Download as PDF 27732 Federal Register / Vol. 72, No. 95 / Thursday, May 17, 2007 / Rules and Regulations TABLE 1.—APPLICABILITY—Continued EMBRAER model— As identified in— EMB–135BJ airplanes .............................................................................. Unsafe Condition (d) This AD results from a report of the failure of a fitting clamp of an electrical bonding cable for the fuel tubing. We are issuing this AD to prevent loss of bonding protection in the interior of the fuel tanks or adjacent areas, and a consequent potential source of ignition in a fuel tank and possible fire or explosion. EMBRAER Service Bulletin 145LEG–28–0030, dated April 19, 2006. Compliance (e) You are responsible for having the actions required by this AD performed within the compliance times specified, unless the actions have already been done. Electrical Bonding Clamp Replacement (f) At the time specified in paragraph (f)(1) or (f)(2) of this AD, as applicable: Replace the electrical bonding clamps having part numbers AN735D6 and AN735D4 inside the forward fuel tank or the ventral, wing stub, and wing fuel tanks, and adjacent areas, as applicable; by accomplishing all actions specified in the Accomplishment Instructions of the applicable service bulletin identified in Table 2 of this AD. TABLE 2.—APPLICABLE SERVICE INFORMATION For EMBRAER model— Use— EMB–145LR, –145XR, –145MP, and –135LR airplanes ......................... EMB–135BJ airplanes .............................................................................. (1) For Model EMB–145LR, –145XR, and –145MP airplanes; and Model EMB–135LR airplanes: Within 5,000 flight hours after the effective date of this AD. (2) For Model EMB–135BJ airplanes: Within 4,000 flight hours or 48 calendar months after the effective date of this AD, whichever occurs first. Alternative Methods of Compliance (AMOCs) EMBRAER Service Bulletin 145–28–0028, dated November 7, 2005 EMBRAER Service Bulletin 145LEG–28–0030, dated April 19, 2006. to: https://www.archives.gov/federal-register/ cfr/ibr-locations.html. Issued in Renton, Washington, on May 7, 2007. Stephen P. Boyd, Acting Manager, Transport Airplane Directorate, Aircraft Certification Service. [FR Doc. E7–9401 Filed 5–16–07; 8:45 am] BILLING CODE 4910–13–P (g)(1) The Manager, International Branch ANM–116, Transport Airplane Directorate, FAA, has the authority to approve AMOCs for this AD, if requested in accordance with the procedures found in 14 CFR 39.19. (2) Before using any AMOC approved in accordance with § 39.19 on any airplane to which the AMOC applies, notify the appropriate principal inspector in the FAA Flight Standards Certificate Holding District Office. DEPARTMENT OF TRANSPORTATION Federal Aviation Administration 14 CFR Parts 401, 415, 431, 435, 440 and 460 [Docket No. FAA–2005–23449] Related Information Human Space Flight Requirements for Crew and Space Flight Participants (h) Brazilian airworthiness directive 2006– 02–03R2, effective October 8, 2006, also addresses the subject of this AD. AGENCY: cprice-sewell on PROD1PC71 with RULES Material Incorporated by Reference (i) You must use EMBRAER Service Bulletin 145–28–0028, dated November 7, 2005; or EMBRAER Service Bulletin 145LEG–28–0030, dated April 19, 2006; as applicable; to perform the actions that are required by this AD, unless the AD specifies otherwise. The Director of the Federal Register approved the incorporation by reference of these documents in accordance with 5 U.S.C. 552(a) and 1 CFR part 51. Contact Empresa Brasileira de Aeronautica S.A. (EMBRAER), P.O. Box 343—CEP 12.225, Sao Jose dos Campos—SP, Brazil, for a copy of this service information. You may review copies at the FAA, Transport Airplane Directorate, 1601 Lind Avenue, SW., Renton, Washington; or at the National Archives and Records Administration (NARA). For information on the availability of this material at NARA, call 202–741–6030, or go VerDate Aug<31>2005 15:37 May 16, 2007 Jkt 211001 Federal Aviation Administration, DOT. ACTION: Notice of Office of Management and Budget Approval for Information Collection. SUMMARY: This notice announces the Office of Management and Budget’s (OMB) approval of the information collection requirement in the final rule published on December 15, 2006. The sections of the final rule pending approval of this information collection request are effective upon publication of this notice. DATES: On April 16, 2007, the FAA received OMB approval for the information collection requirement in the final rule published at 71 FR 75616 (December 15, 2006). The compliance date for information collection requirements in §§ 460.5, 460.7, 460.9, PO 00000 Frm 00012 Fmt 4700 Sfmt 4700 460.19, 460.45, and 460.49 is May 17, 2007. FOR FURTHER INFORMATION CONTACT: For technical information, contact Kenneth Wong, Deputy Manager, Licensing and Safety Division, Commercial Space Transportation, AST–200, Federal Aviation Administration, 800 Independence Avenue, SW., Washington, DC 20591; telephone (202) 267–8465; facsimile (202) 267–3686; e-mail ken.wong@faa.gov. For legal information, contact Laura Montgomery, Senior Attorney, Office of the Chief Counsel, Federal Aviation Administration, 800 Independence Avenue, SW., Washington, DC 20591; telephone (202) 267–3150; facsimile (202) 267–7971, e-mail laura.montgomery@faa.gov. SUPPLEMENTARY INFORMATION: Background On December 15, 2006, the FAA published the final rule, Human Space Flight Requirements for Crew and Space Flight Participants, in the Federal Register. The rule established requirements for human space flight as required by the Commercial Space Launch Amendments Act of 2004. In the DATES section of the final rule, we noted that affected parties did not need to comply with the information collection requirements in specified sections of the rule until the Office of Management and Budget (OMB) approved the FAA’s request to collect the information. According to the Paperwork Reduction Act, OMB approved the FAA’s request for new information collection on April 16, 2007, and assigned the information collection OMB Control Number 2120–0720. The E:\FR\FM\17MYR1.SGM 17MYR1 Federal Register / Vol. 72, No. 95 / Thursday, May 17, 2007 / Rules and Regulations control number was not available when the final rule was published, thus necessitating publication of this notice. The FAA request was approved by OMB without change and expires on April 30, 2010. Title 49 U.S.C. 106(g), 40113, 40119, 41706, 44101, 44701–44702, 44705, 44709–44711, 44713, 44716–44717, 44722, 46105, grants authority to the Administrator to publish this notice. The final rule (71 FR 75616) became effective on February 13, 2007 and the compliance date for information collection requirements in §§ 460.5, 460.7, 460.9, 460.19, 460.45, and 460.49 is May 17, 2007. Issued in Washington, DC on May 8, 2007. Pamela Hamilton-Powell, Director, Office of Rulemaking Aviation Safety. [FR Doc. E7–9480 Filed 5–16–07; 8:45 am] BILLING CODE 4910–13–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 520 Oral Dosage Form New Animal Drugs; Pimobendan AGENCY: Food and Drug Administration, HHS. cprice-sewell on PROD1PC71 with RULES ACTION: Final rule. SUMMARY: The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of a new animal drug application (NADA) filed by Boehringer Ingelheim Vetmedica, Inc. The NADA provides for the veterinary prescription use of pimobendan chewable tablets in dogs for the management of the signs of congestive heart failure. DATES: This rule is effective May 17, 2007. FOR FURTHER INFORMATION CONTACT: Melanie R. Berson, Center for Veterinary Medicine (HFV–110), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 301–827–7540, email: melanie.berson@fda.hhs.gov. SUPPLEMENTARY INFORMATION: Boehringer Ingelheim Vetmedica, Inc., 2621 N. Belt Hwy., St. Joseph, MO 64506–2002, filed NADA 141–273 that provides for the veterinary prescription use of VETMEDIN (pimobendan) Chewable Tablets in dogs for the management of the signs of mild, moderate, or severe (modified New York Heart Association Class II, III, or IV) congestive heart failure due to VerDate Aug<31>2005 15:37 May 16, 2007 Jkt 211001 atrioventricular valvular insufficiency or dilated cardiomyopathy; for use with concurrent therapy for congestive heart failure as appropriate on a case-by-case basis. The NADA is approved as of April 30, 2007, and the regulations in 21 CFR part 520 are amended by adding § 520.1780 to reflect the approval. 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)(i) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360b(c)(2)(F)(i)), this approval qualifies for 5 years of marketing exclusivity beginning on the date of the approval. The agency has determined under 21 CFR 25.33(d)(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 520 Animal drugs. I 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 520 is amended as follows: PART 520—ORAL DOSAGE FORM NEW ANIMAL DRUGS 1. The authority citation for 21 CFR part 520 continues to read as follows: I Authority: 21 U.S.C. 360b. I 2. Add § 520.1780 to read as follows: § 520.1780 Pimobendan. (a) Specifications. Each chewable tablet contains 1.25, 2.5, or 5 milligrams (mg) pimobendan. (b) Sponsor. See No. 000010 in § 510.600(c) of this chapter. (c) Conditions of use in dogs—(1) Amount. Administer orally at a total daily dose of 0.23 mg per pound (0.5 mg per kilogram) body weight, using a suitable combination of whole or half PO 00000 Frm 00013 Fmt 4700 Sfmt 4700 27733 tablets. The total daily dose should be divided into two portions administered approximately 12 hours apart. (2) Indications for use. For the management of the signs of mild, moderate, or severe (modified New York Heart Association Class II, III, or IV) congestive heart failure due to atrioventricular valvular insufficiency or dilated cardiomyopathy; for use with concurrent therapy for congestive heart failure as appropriate on a case-by-case basis. (3) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Dated: May 7, 2007. Bernadette Dunham, Deputy Director, Center for Veterinary Medicine. [FR Doc. E7–9516 Filed 5–16–07; 8:45 am] BILLING CODE 4160–01–S DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 21 CFR Part 522 Implantation or Injectable Dosage Form New Animal Drugs; Ivermectin and Clorsulon AGENCY: Food and Drug Administration, HHS. ACTION: Final rule. SUMMARY: The Food and Drug Administration (FDA) is amending the animal drug regulations to reflect approval of an abbreviated new animal drug application (ANADA) filed by Norbrook Laboratories, Ltd. The ANADA provides for the use of an ivermectin and clorsulon solution by subcutaneous injection in cattle for control of various internal and external parasites. DATES: This rule is effective May 17, 2007. John K. Harshman, Center for Veterinary Medicine (HFV–104), Food and Drug Administration, 7500 Standish Pl., Rockville, MD 20855, 301–827–0169, email: john.harshman@fda.hhs.gov. SUPPLEMENTARY INFORMATION: Norbrook Laboratories, Ltd., Station Works, Newry BT35 6JP, Northern Ireland, filed ANADA 200–436 that provides for use of NOROMECTIN Plus (ivermectin and clorsulon) Injection for Cattle by subcutaneous injection in cattle for control of various internal and external parasites. Norbrook Laboratories, Ltd.’s NOROMECTIN Plus Injection for Cattle FOR FURTHER INFORMATION CONTACT: E:\FR\FM\17MYR1.SGM 17MYR1

Agencies

[Federal Register Volume 72, Number 95 (Thursday, May 17, 2007)]
[Rules and Regulations]
[Pages 27732-27733]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-9480]


-----------------------------------------------------------------------

DEPARTMENT OF TRANSPORTATION

Federal Aviation Administration

14 CFR Parts 401, 415, 431, 435, 440 and 460

[Docket No. FAA-2005-23449]


Human Space Flight Requirements for Crew and Space Flight 
Participants

AGENCY: Federal Aviation Administration, DOT.

ACTION: Notice of Office of Management and Budget Approval for 
Information Collection.

-----------------------------------------------------------------------

SUMMARY: This notice announces the Office of Management and Budget's 
(OMB) approval of the information collection requirement in the final 
rule published on December 15, 2006. The sections of the final rule 
pending approval of this information collection request are effective 
upon publication of this notice.

DATES: On April 16, 2007, the FAA received OMB approval for the 
information collection requirement in the final rule published at 71 FR 
75616 (December 15, 2006). The compliance date for information 
collection requirements in Sec. Sec.  460.5, 460.7, 460.9, 460.19, 
460.45, and 460.49 is May 17, 2007.

FOR FURTHER INFORMATION CONTACT: For technical information, contact 
Kenneth Wong, Deputy Manager, Licensing and Safety Division, Commercial 
Space Transportation, AST-200, Federal Aviation Administration, 800 
Independence Avenue, SW., Washington, DC 20591; telephone (202) 267-
8465; facsimile (202) 267-3686; e-mail ken.wong@faa.gov. For legal 
information, contact Laura Montgomery, Senior Attorney, Office of the 
Chief Counsel, Federal Aviation Administration, 800 Independence 
Avenue, SW., Washington, DC 20591; telephone (202) 267-3150; facsimile 
(202) 267-7971, e-mail laura.montgomery@faa.gov.

SUPPLEMENTARY INFORMATION:

Background

    On December 15, 2006, the FAA published the final rule, Human Space 
Flight Requirements for Crew and Space Flight Participants, in the 
Federal Register. The rule established requirements for human space 
flight as required by the Commercial Space Launch Amendments Act of 
2004. In the DATES section of the final rule, we noted that affected 
parties did not need to comply with the information collection 
requirements in specified sections of the rule until the Office of 
Management and Budget (OMB) approved the FAA's request to collect the 
information.
    According to the Paperwork Reduction Act, OMB approved the FAA's 
request for new information collection on April 16, 2007, and assigned 
the information collection OMB Control Number 2120-0720. The

[[Page 27733]]

control number was not available when the final rule was published, 
thus necessitating publication of this notice. The FAA request was 
approved by OMB without change and expires on April 30, 2010.
    Title 49 U.S.C. 106(g), 40113, 40119, 41706, 44101, 44701-44702, 
44705, 44709-44711, 44713, 44716-44717, 44722, 46105, grants authority 
to the Administrator to publish this notice. The final rule (71 FR 
75616) became effective on February 13, 2007 and the compliance date 
for information collection requirements in Sec. Sec.  460.5, 460.7, 
460.9, 460.19, 460.45, and 460.49 is May 17, 2007.

    Issued in Washington, DC on May 8, 2007.
Pamela Hamilton-Powell,
Director, Office of Rulemaking Aviation Safety.
[FR Doc. E7-9480 Filed 5-16-07; 8:45 am]
BILLING CODE 4910-13-P
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.