Manufacturer of Controlled Substances; Notice of Registration, 9967 [E7-3919]

Download as PDF 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