80_FR_15688 80 FR 15632 - Bulk Manufacturer of Controlled Substances Application: Penick Corporation

80 FR 15632 - Bulk Manufacturer of Controlled Substances Application: Penick Corporation

DEPARTMENT OF JUSTICE
Drug Enforcement Administration

Federal Register Volume 80, Issue 56 (March 24, 2015)

Page Range15632-15632
FR Document2015-06734

Federal Register, Volume 80 Issue 56 (Tuesday, March 24, 2015) 
[Federal Register Volume 80, Number 56 (Tuesday, March 24, 2015)]
[Notices]
[Page 15632]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2015-06734]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Penick 
Corporation

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and 
applicants therefore, may file written comments on or objections to the 
issuance of the proposed registration in accordance with 21 CFR 
1301.33(a) on or before May 26, 2015.

ADDRESSES:  Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/ODW, 
8701 Morrissette Drive, Springfield, Virginia 22152. Request for 
hearings should be sent to: Drug Enforcement Administration, Attention: 
Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: The Attorney General has delegated his 
authority under the Controlled Substances Act to the Administrator of 
the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority 
to exercise all necessary functions with respect to the promulgation 
and implementation of 21 CFR part 1301, incident to the registration of 
manufacturers, distributors, dispensers, importers, and exporters of 
controlled substances (other than final orders in connection with 
suspension, denial, or revocation of registration) has been redelegated 
to the Deputy Assistant Administrator of the DEA Office of Diversion 
Control (``Deputy Assistant Administrator'') pursuant to section 7 of 
28 CFR part 0, appendix to subpart, R.
    In accordance with 21 CFR 1301.33(a), this is notice that on 
February 26, 2014, Penick Corporation, 33 Industrial Park Road, 
Pennsville, New Jersey 08070, applied to be registered as a bulk 
manufacturer of the following basic classes of controlled substances:

 
------------------------------------------------------------------------
            Controlled substance                       Schedule
------------------------------------------------------------------------
Cocaine (9041).............................  II
Codeine (9050).............................  II
Dihydrocodeine (9120)......................  II
Oxycodone (9143)...........................  II
Hydromorphone (9150).......................  II
Ecgonine (9180)............................  II
Hydrocodone (9193).........................  II
Morphine (9300)............................  II
Oripavine (9330)...........................  II
Thebaine (9333)............................  II
Opium tincture (9630)......................  II
Oxymorphone (9652).........................  II
------------------------------------------------------------------------

    The company plans to manufacture the above-listed controlled 
substances as bulk controlled substance intermediates for distribution 
to its customers.

    Dated: March 9, 2015.
Joseph T. Rannazzisi,
Deputy Assistant Administrator.
[FR Doc. 2015-06734 Filed 3-23-15; 8:45 am]
BILLING CODE 4410-09-P

15632 Federal Register / Vol. 80, No. 56 / Tuesday, March 24, 2015 / Notices DEPARTMENT OF JUSTICE DEPARTMENT OF JUSTICE Drug Enforcement Administration Drug Enforcement Administration Controlled substance Schedule [Docket No. DEA–392] Thebaine (9333) ........................... II [Docket No. DEA–392] Opium tincture (9630) .................. II Bulk Manufacturer of Controlled Oxymorphone (9652) ................... II Bulk Manufacturer of Controlled Substances Application: Penick Substances Application: Patheon Corporation The company plans to manufacture Pharmaceuticals, Inc. the above-listed controlled substances ACTION: Notice of application. as bulk controlled substance ACTION: Notice of application. intermediates for distribution to its DATES: Registered bulk manufacturers of customers. DATES: Registered bulk manufacturers of the affected basic classes, and Dated: March 9, 2015. the affected basic class and applicants applicants therefore, may file written Joseph T. Rannazzisi, therefore may file written comments or comments on or objections to the issuance of the proposed registration in Deputy Assistant Administrator. objections to the issuance of the [FR Doc. 2015–06734 Filed 3–23–15; 8:45 am] proposed registration in accordance accordance with 21 CFR 1301.33(a) on with 21 CFR 1301.33(a) on or before or before May 26, 2015. BILLING CODE 4410–09–P May 26, 2015. ADDRESSES: Written comments should be sent to: Drug Enforcement ADDRESSES: Written comments should Administration, Attention: DEA Federal LIBRARY OF CONGRESS be sent to: Drug Enforcement Register Representative/ODW, 8701 Administration, Attention: DEA Federal Copyright Royalty Board Morrissette Drive, Springfield, Virginia Register Representative/ODW, 8701 22152. Request for hearings should be [Docket No. 14–CRB–0006 DART SR (CO/ Morrissette Drive, Springfield, Virginia sent to: Drug Enforcement FA) 2013] 22152. Request for hearings should be Administration, Attention: Hearing sent to: Drug Enforcement Clerk/LJ, 8701 Morrissette Drive, Distribution of the 2013 Digital Audio Administration, Attention: Hearing Springfield, Virginia 22152. Recording Technology Royalty Funds Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The AGENCY: Copyright Royalty Board, Attorney General has delegated his Library of Congress. SUPPLEMENTARY INFORMATION: The authority under the Controlled ACTION: Notice announcing Attorney General has delegated his Substances Act to the Administrator of commencement of proceeding with authority under the Controlled the Drug Enforcement Administration request for Petitions to Participate and Substances Act to the Administrator of (DEA), 28 CFR 0.100(b). Authority to comments on intention to conduct the Drug Enforcement Administration exercise all necessary functions with paper proceeding. (DEA), 28 CFR 0.100(b). Authority to respect to the promulgation and exercise all necessary functions with implementation of 21 CFR part 1301, SUMMARY: The Copyright Royalty Board respect to the promulgation and incident to the registration of is announcing the commencement of a implementation of 21 CFR part 1301, manufacturers, distributors, dispensers, proceeding to determine the distribution incident to the registration of importers, and exporters of controlled of the digital audio recording manufacturers, distributors, dispensers, substances (other than final orders in technology royalty fees in the 2013 importers, and exporters of controlled connection with suspension, denial, or Sound Recordings Fund (Copyright substances (other than final orders in revocation of registration) has been Owners and Featured Recording Artists connection with suspension, denial, or redelegated to the Deputy Assistant Subfunds). The Board is also revocation of registration) has been Administrator of the DEA Office of announcing the date by which a party redelegated to the Deputy Assistant Diversion Control (‘‘Deputy Assistant who wishes to participate in this Administrator of the DEA Office of Administrator’’) pursuant to section 7 of proceeding must file its Petition to Diversion Control (‘‘Deputy Assistant 28 CFR part 0, appendix to subpart, R. Participate and the accompanying $150 Administrator’’) pursuant to section 7 of In accordance with 21 CFR filing fee, if applicable. Finally, the 28 CFR part 0, appendix to subpart R. 1301.33(a), this is notice that on Board is announcing the Copyright In accordance with 21 CFR February 26, 2014, Penick Corporation, Royalty Judges’ intention to conduct a 1301.33(a), this is notice that on 33 Industrial Park Road, Pennsville, paper proceeding. December 11, 2014, Patheon New Jersey 08070, applied to be DATES: Petitions to Participate, Pharmaceuticals, Inc., 2110 E. Galbraith registered as a bulk manufacturer of the comments on the intention to conduct a Road, Cincinnati, Ohio 45237 applied to following basic classes of controlled paper proceeding, and applicable filing be registered as a bulk manufacturer of substances: fee are due no later than April 23, 2015. gamma hydroxybutyric acid (2010), a ADDRESSES: An original, five copies, and basic class of nonnarcotic controlled an electronic copy in Portable substance in schedule I. Controlled substance Schedule Document Format (PDF) on a CD of the The company plans to manufacture Petition to Participate, along with the Cocaine (9041) ............................. II mstockstill on DSK4VPTVN1PROD with NOTICES the listed controlled substance for $150 filing fee, if applicable, may be Codeine (9050) ............................. II delivered to the Copyright Royalty distribution to its customers. Dihydrocodeine (9120) ................. II Board by either mail or hand delivery. Dated: March 9, 2015. Oxycodone (9143) ........................ II Hydromorphone (9150) ................ II Petitions to Participate and the $150 Joseph T. Rannazzisi, filing fee may not be delivered by an Ecgonine (9180) ........................... II Deputy Assistant Administrator. Hydrocodone (9193) ..................... II overnight delivery service other than the [FR Doc. 2015–06733 Filed 3–23–15; 8:45 am] Morphine (9300) ........................... II U.S. Postal Service Express Mail. If by BILLING CODE 4410–09–P Oripavine (9330) ........................... II mail (including overnight delivery), VerDate Sep<11>2014 01:09 Mar 24, 2015 Jkt 235001 PO 00000 Frm 00085 Fmt 4703 Sfmt 4703 E:\FR\FM\24MRN1.SGM 24MRN1


Document Created: 2015-12-18 11:44:56
Document Modified: 2015-12-18 11:44:56
CategoryRegulatory Information
CollectionFederal Register
sudoc ClassAE 2.7:
GS 4.107:
AE 2.106:
PublisherOffice of the Federal Register, National Archives and Records Administration
SectionNotices
ActionNotice of application.
DatesRegistered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before May 26, 2015.
FR Citation80 FR 15632 
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