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10068 Federal Register / Vol. 76, No. 36 / Wednesday, February 23, 2011 / Notices

Drug Schedule registration to import a basic class of Dated: February 15, 2011. any controlled substance in schedule I Joseph T. Rannazzisi, (7434) ...... I or II are, and will continue to be, Deputy Assistant Administrator, Office of Dimethyltryptamine (7435) ...... I required to demonstrate to the Deputy Diversion Control, Drug Enforcement (7437) ...... I Assistant Administrator, Office of Administration. Psilocyn (7438) ...... I [FR Doc. 2011–3948 Filed 2–22–11; 8:45 am] 1-[1-(2- I Diversion Control, Drug Enforcement Thienyl)cyclohexyl]piperidine Administration, that the requirements BILLING CODE 4410–09–P (7470). for such registration pursuant to 21 N- (BZP) (7493) I U.S.C. 958(a); 21 U.S.C. 823(a); and 21 (9200) ...... I CFR 1301.34(b), (c), (d), (e), and (f) are DEPARTMENT OF JUSTICE (9313) ...... I satisfied. (9624) ...... I Drug Enforcement Administration Amphetamine (1100) ...... II Dated: February 15, 2011. Methamphetamine (1105) ...... II Joseph T. Rannazzisi, Manufacturer of Controlled Methylphenidate (1724) ...... II Substances; Notice of Application Deputy Assistant Administrator, Office of Amobarbital (2125) ...... II Diversion Control, Drug Enforcement Pentobarbital (2270) ...... II Administration. Pursuant to § 1301.33(a), Title 21 of Secobarbital (2315) ...... II the Code of Federal Regulations (CFR), [FR Doc. 2011–3945 Filed 2–22–11; 8:45 am] Glutethimide (2550) ...... II this is notice that on January 6, 2011, (7379) ...... II BILLING CODE 4410–09–P Johnson Matthey Pharmaceutical (7471) ...... II Cocaine (9041) ...... II Materials Inc., Pharmaceutical Service, 25 Patton Road, Devens, Massachusetts (9050) ...... II DEPARTMENT OF JUSTICE Diprenorphine (9058) ...... II 01434, made application by renewal to (9143) ...... II Drug Enforcement Administration the Drug Enforcement Administration (9150) ...... II (DEA) to be registered as a bulk (9170) ...... II Importer of Controlled Substances; manufacturer of the following basic Ecgonine (9180) ...... II classes of controlled substances: (9190) ...... II Notice of Registration (9193) ...... II Drug Schedule (9220) ...... II By Notice dated November 1, 2010, Meperidine (9230) ...... II and published in the Federal Register Amphetamine (1100) ...... II (9250) ...... II on November 12, 2010, 75 FR 69461, Methylphenidate (1724) ...... II (9300) ...... II Wildlife Laboratories, 1401 Duff Drive, Nabilone (7379) ...... II (9333) ...... II Suite 400, Fort Collins, Colorado 80524, (9737) ...... II , powdered (9639) ...... II made application by renewal to the (9740) ...... II Levo- (9648) .. II Hydrocodone (9193) ...... II (9652) ...... II Drug Enforcement Administration (9801) ...... II (DEA) to be registered as an importer of Hydrochloride (9059), a basic The company plans to utilize this The company plans to import the class of controlled substance listed in facility to manufacture small quantities listed controlled substances for sale to schedule II. of the listed controlled substances in research facilities for drug testing and The company plans to import the bulk and to conduct analytical testing in analysis. listed controlled substance for sale to its support of the company’s primary Any bulk manufacturer who is customer. manufacturing facility in West Deptford, presently, or is applying to be, New Jersey. The controlled substances registered with DEA to manufacture No comments or objections have been manufactured in bulk at this facility will such basic classes of controlled received. DEA has considered the be distributed to the company’s substances may file comments or factors in 21 U.S.C. 823(a) and § 952(a) customers. and determined that the registration of objections to the issuance of the Any other such applicant, and any Wildlife Laboratories to import the basic proposed registration and may, at the person who is presently registered with class of controlled substance is same time, file a written request for a DEA to manufacture such substances, consistent with the public interest and hearing on such application pursuant to may file comments or objections to the 21 CFR 1301.43, and in such form as with United States obligations under issuance of the proposed registration prescribed by 21 CFR 1316.47. international treaties, conventions, or pursuant to 21 CFR 1301.33(a). Any such comments or objections protocols in effect on May 1, 1971. DEA Any such written comments or should be addressed, in quintuplicate, has investigated Wildlife Laboratories to objections should be addressed, in to the Drug Enforcement ensure that the company’s registration is quintuplicate, to the Drug Enforcement Administration, Office of Diversion consistent with the public interest. The Administration, Office of Diversion Control, Federal Register Representative investigation has included inspection Control, Federal Register Representative (ODL), 8701 Morrissette Drive, and testing of the company’s physical (ODL), 8701 Morrissette Drive, Springfield, Virginia 22152; and must be security systems, verification of the Springfield, Virginia 22152; and must be filed no later than [insert date 30 days company’s compliance with State and filed no later than April 25, 2011. from date of publication]. local laws, and a review of the This procedure is to be conducted company’s background and history. Dated: February 15, 2011. simultaneously with, and independent Therefore, pursuant to 21 U.S.C. 952(a) Joseph T. Rannazzisi, of, the procedures described in 21 CFR and 958(a), and in accordance with 21 Deputy Assistant Administrator, Office of 1301.34(b), (c), (d), (e), and (f). As noted CFR 1301.34, the above named company Diversion Control, Drug Enforcement in a previous notice published in the is granted registration as an importer of Administration. Federal Register on September 23, 1975, the basic class of controlled substance [FR Doc. 2011–3928 Filed 2–22–11; 8:45 am] (40 FR 43745–46), all applicants for listed. BILLING CODE 4410–09–P

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