Manufacturer of Controlled Substances; Notice of Application, 43211-43212 [E6-12174]

Download as PDF 43211 Federal Register / Vol. 71, No. 146 / Monday, July 31, 2006 / Notices Enforcement Administration (DEA) for registration as an importer of Marihuana (7360), a basic class of controlled substance in Schedule I. The company plans to import a finished pharmaceutical product containing cannabis extracts in dosage form for packaging for a clinical trial study. Any manufacturer who is presently, or is applying to be, registered with DEA to manufacture such basic classes of controlled substances may file comments or objections to the issuance of the proposed registration and may, at the same time, file a written request for a hearing on such application pursuant to 21 CFR 1301.43 and in such form as prescribed by 21 CFR 1316.47. Any such written comments or objections being sent via regular mail should be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative/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 August 30, 2006. This procedure is to be conducted simultaneously with and independent of the procedures described in 21 CFR 1301.34(b), (c), (d), (e) and (f). As noted in a previous notice published in the Federal Register on September 23, 1975, (40 FR 43745–46), all applicants for registration to import a basic class of any controlled substance listed in Schedule I or II are, and will continue to be required to demonstrate to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, that the requirements for such registration pursuant to 21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR 301.34(b), (c), (d), (e) and (f) are satisfied. Dated: July 25, 2006. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E6–12171 Filed 7–28–06; 8:45 am] BILLING CODE 4410–09–P (CFR), this is notice that on October 28, 2005, MGI Pharma, 6611 Tributary Street, Baltimore, Maryland 21224, made application to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Cocaine (9041), a basic class of controlled substance listed in Schedules II. The company plans to manufacture a cocaine derivative to be used in domestic and foreign clinical research studies. 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 should be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative/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 September 29, 2006. Dated: July 25, 2006. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E6–12172 Filed 7–28–06; 8:45 am] sroberts on PROD1PC70 with NOTICES Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations VerDate Aug<31>2005 17:34 Jul 28, 2006 Jkt 208001 II II II The company plans to manufacture the listed controlled substances as bulk controlled substance intermediates for distribution to its customers for further manufacture or to manufacture pharmaceutical dosage forms. 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 should be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative/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 September 29, 2006. Dated: July 25, 2006. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E6–12173 Filed 7–28–06; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE DEPARTMENT OF JUSTICE Drug Enforcement Administration Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Manufacturer of Controlled Substances; Notice of Application Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on March 22, 2006, Penick Corporation, 33 Industrial Park Road, Pennsville, New Jersey 08070, 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 Manufacturer of Controlled Substances; Notice of Application Morphine (9300) ........................... Thebaine (9333) ........................... Oxymorphone (9652) ................... Schedule BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Drug Frm 00118 Fmt 4703 Drug Schedule Cocaine (9041) ............................. Codeine (9050) ............................. Dihydrocodeine (9120) ................. Oxycodone (9143) ........................ Hydromorphone (9150) ................ Ecgonine (9180) ........................... Hydrocodone (9193) ..................... PO 00000 Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on January 26, 2006, Roche Diagnostics Operations Inc., Attn: Regulatory Compliance, 9115 Hague Road, Indianapolis, Indiana 46250, 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 I and II: Sfmt 4703 II II II II II II II Lysergic Acid Diethylamide (7315) Tetrahydrocannabinol (7370) ....... Alphamethadol (9605) .................. Phencyclidine (7471) .................... Ecgonine (9180) ........................... Methadone (9250) ........................ Morphine (9300) ........................... E:\FR\FM\31JYN1.SGM 31JYN1 Schedule I I I II II II II 43212 Federal Register / Vol. 71, No. 146 / Monday, July 31, 2006 / Notices The company plans to manufacture small quantities of the listed controlled substances for use in diagnostic products. 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 September 29, 2006. Dated: July 25, 2006. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E6–12174 Filed 7–28–06; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF LABOR Employment and Training Administration [TA–W–59,628] sroberts on PROD1PC70 with NOTICES Cadence Innovation, New Venture Industries, Grand Blanc, MI; Notice of Termination of Investigation Pursuant to section 221 of the Trade Act of 1974, as amended, an investigation was initiated on June 26, 2006 in response to a petition filed by the United Automobile, Aerospace & Agricultural Implement Workers of America International Union 1C and Local Union 524, on behalf of workers of Cadence Innovation, New Venture Industries, Grand Blanc, Michigan. The petitioning worker group is covered by an active certification, TA– W–58,625 (amended July 6, 2006), which does not expire until February 23, 2008. Consequently, further investigation in this case would serve no purpose, and the investigation has been terminated. VerDate Aug<31>2005 17:34 Jul 28, 2006 Jkt 208001 Signed in Washington, DC, this 7th day of July 2006. Linda G. Poole, Certifying Officer, Division of Trade Adjustment Assistance. [FR Doc. E6–12202 Filed 7–28–06; 8:45 am] DEPARTMENT OF LABOR Employment and Training Administration [TA–W–58,815] Coating and Assembly, Inc., Mt. Pleasant, MI; Affirmative Determinations for Worker Adjustment Assistance and Alternative Trade Adjustment Assistance; Correction This notice rescinds the notice of certification of eligibility to apply for Alternative Trade Adjustment Assistance applicable to TA–W–58,815, which was published in the Federal Register on April 13, 2006 (71 FR 19208–19210) in Document E–5518, Billing Code 4510–30–P. This rescinds the certification of eligibility for workers of TA–W–58,815, to apply for Alternative Trade Adjustment Assistance and confirms eligibility to apply for Worker Adjustment Assistance as identified on page 19209 in the first column, the seventh TA–W–number listed. The Department appropriately published in the Federal Register April 13, 2006, page 19210, under the notice of Negative Determinations for Alternative Trade Adjustment Assistance, the denial of eligibility applicable to workers of TA–W–58,815. The notice appears on page 19210 in the third column, the seventh TA–W– number listed. Signed in Washington, DC, this 24th day of July 2006. Erica R. Cantor, Director, Division of Trade Adjustment Assistance. [FR Doc. E6–12195 Filed 7–28–06; 8:45 am] PO 00000 Employment and Training Administration [TA–W–56,258] Collins And Aikman Products Company, Division 016, Roxboro, NC (Including Employees Working Out of Troy, MI); Notice of Revised Determination of Alternative Trade Adjustment Assistance on Reconsideration BILLING CODE 4510–30–P BILLING CODE 4510–30–P DEPARTMENT OF LABOR On February 24, 2005, workers and former workers of Collins and Aikman Products Company, Division 016, Roxboro, North Carolina (subject firm) were certified eligible to apply for Trade Adjustment Assistance (TAA) but not Alternative Trade Adjustment Assistance (ATAA). The Notice of determination was published in the Federal Register on April 1, 2005 (70 FR 16847). An amendment was issued on June 6, 2006 to include employees working out of Troy, Michigan. The Notice of amendment was published in the Federal Register on June 22, 2006 (71 FR 35951). Based on information produced on the initial investigation that workers the subject workers possess skills that are easily transferable, the workers were denied eligibility to apply for ATAA. Administrative reconsideration was not requested. After the Notice of amendment was issued, the Department received new information indicating that the subject workers may possess skills that are not easily transferable. As such, the Department reopened the investigation. Based on information obtain during the reconsideration investigation, the Department determines that the subject workers do not possess skills that are easily transferable. At least five percent of the workforce at the subject from is at least fifty years of age. Competitive conditions within the industry are adverse. Conclusion After careful review of the additional facts obtained on reconsideration, I conclude that the requirements of Section 246 of the Trade Act of 1974, as amended, have been met for the workers of the subject firm. In accordance with the provisions of the Act, I make the following certification: All workers of Collins and Aikman Products Company, Division 016, Roxboro, North Carolina, including employees working out of Troy, Michigan, who became totally or partially separated from employment on or after December 13, 2003 through February 24, 2007, are eligible to Frm 00119 Fmt 4703 Sfmt 4703 E:\FR\FM\31JYN1.SGM 31JYN1

Agencies

[Federal Register Volume 71, Number 146 (Monday, July 31, 2006)]
[Notices]
[Pages 43211-43212]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-12174]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on January 26, 2006, Roche 
Diagnostics Operations Inc., Attn: Regulatory Compliance, 9115 Hague 
Road, Indianapolis, Indiana 46250, 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 I and II:

------------------------------------------------------------------------
                    Drug                               Schedule
------------------------------------------------------------------------
Lysergic Acid Diethylamide (7315)..........  I
Tetrahydrocannabinol (7370)................  I
Alphamethadol (9605).......................  I
Phencyclidine (7471).......................  II
Ecgonine (9180)............................  II
Methadone (9250)...........................  II
Morphine (9300)............................  II
------------------------------------------------------------------------


[[Page 43212]]

    The company plans to manufacture small quantities of the listed 
controlled substances for use in diagnostic products.
    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 September 29, 2006.

    Dated: July 25, 2006.
 Joseph T. Rannazzisi,
 Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
 [FR Doc. E6-12174 Filed 7-28-06; 8:45 am]
BILLING CODE 4410-09-P
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