Importer of Controlled Substances Application: Wildlife Laboratories, Inc., 14914 [2017-05729]

Download as PDF 14914 Federal Register / Vol. 82, No. 55 / Thursday, March 23, 2017 / Notices Company FR docket Fisher Clinical Services, Inc .......................................................................................................................... Sigma-Aldrich International: GMBH-Sigma Aldrich Company LLC ..................................................................................................... Fisher Clinical Services, Inc ................................................................................................................... Anderson Brecon, Inc ............................................................................................................................ Johnson Matthey Inc .............................................................................................................................. Wildlife Laboratories, Inc ........................................................................................................................ Noramco, Inc .......................................................................................................................................... Mylan Technologies, Inc ........................................................................................................................ 81 FR 61248 September 6, 2016. 81 81 81 81 81 81 82 September 14, 2016. October 4, 2016. October 18, 2016. October 18, 2016. December 28, 2016. December 28, 2016. January 23, 2017. The DEA has considered the factors in 21 U.S.C. 823, 952(a) and 958(a) and determined that the registration of the listed registrants to import the applicable basic classes of schedule I or II controlled substances is consistent with the public interest and with United States obligations under international treaties, conventions, or protocols in effect on May 1, 1971. The DEA investigated each company’s maintenance of effective controls against diversion by inspecting and testing each company’s physical security systems, verifying each company’s compliance with state and local laws, and reviewing each company’s background and history. Therefore, pursuant to 21 U.S.C. 952(a) and 958(a), and in accordance with 21 CFR 1301.34, the DEA has granted a registration as an importer for schedule I or II controlled substances to the above listed persons. Dated: March 17, 2017. Louis J. Milione, Assistant Administrator. [FR Doc. 2017–05730 Filed 3–22–17; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–392] Importer of Controlled Substances Application: Wildlife Laboratories, Inc. ACTION: Notice of application. 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 1301.34(a) on or before April 24, 2017. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before April 24, 2017. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette DATES: FR FR FR FR FR FR FR 63223 68455 71766 71766 95644 95640 7859 Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Attn: DEA Federal Register Representative/DRW, 8701 Morrissette Drive, Springfield, Virginia 22152. 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 Assistant Administrator of the DEA Diversion Control Division (‘‘Assistant Administrator’’) pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.34(a), this is notice that on February 2, 2017, Wildlife Laboratories, Inc., 1230 W. Ash Street, Suite D, Windsor, Colorado 80550–8055 applied to be registered as an importer of the following basic classes of controlled substances: SUPPLEMENTARY INFORMATION: Controlled substance Drug code Etorphine (except HCl) ............................................................................................................................................ Etorphine HCl .......................................................................................................................................................... Thiafentanil .............................................................................................................................................................. sradovich on DSK3GMQ082PROD with NOTICES The company plans to import the listed controlled substances for sale to its customers. DEPARTMENT OF LABOR Dated: March 17, 2017. Louis J. Milione, Assistant Administrator. Agency Information Collection Activities; Submission for OMB Review; Comment Request; FederalState Unemployment Insurance Program Data Exchange Standardization [FR Doc. 2017–05729 Filed 3–22–17; 8:45 am] BILLING CODE 4410–09–P Office of the Secretary ACTION: Notice. 18:27 Mar 22, 2017 Jkt 241001 PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 Schedule 9056 9059 9729 I II II and Training Administration (ETA) sponsored information collection request (ICR) titled, ‘‘Federal-State Unemployment Insurance Program Data Exchange Standardization,’’ to the Office of Management and Budget (OMB) for review and approval for continued use, without change, in accordance with the Paperwork Reduction Act of 1995 (PRA). Public comments on the ICR are invited. The OMB will consider all written comments that agency receives on or before April 24, 2017. DATES: The Department of Labor (DOL) is submitting the Employment SUMMARY: VerDate Sep<11>2014 Published E:\FR\FM\23MRN1.SGM 23MRN1

Agencies

[Federal Register Volume 82, Number 55 (Thursday, March 23, 2017)]
[Notices]
[Page 14914]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-05729]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Importer of Controlled Substances Application: Wildlife 
Laboratories, Inc.

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 
1301.34(a) on or before April 24, 2017. Such persons may also file a 
written request for a hearing on the application pursuant to 21 CFR 
1301.43 on or before April 24, 2017.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DRW, 
8701 Morrissette Drive, Springfield, Virginia 22152. All requests for 
hearing must be sent to: Drug Enforcement Administration, Attn: 
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All 
requests for hearing should also be sent to: (1) Drug Enforcement 
Administration, Attn: Hearing Clerk/LJ, 8701 Morrissette Drive, 
Springfield, Virginia 22152; and (2) Drug Enforcement Administration, 
Attn: DEA Federal Register Representative/DRW, 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 Assistant Administrator of the DEA Diversion Control Division 
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, 
appendix to subpart R.
    In accordance with 21 CFR 1301.34(a), this is notice that on 
February 2, 2017, Wildlife Laboratories, Inc., 1230 W. Ash Street, 
Suite D, Windsor, Colorado 80550-8055 applied to be registered as an 
importer of the following basic classes of controlled substances:

------------------------------------------------------------------------
          Controlled substance               Drug code       Schedule
------------------------------------------------------------------------
Etorphine (except HCl)..................            9056               I
Etorphine HCl...........................            9059              II
Thiafentanil............................            9729              II
------------------------------------------------------------------------

    The company plans to import the listed controlled substances for 
sale to its customers.

    Dated: March 17, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017-05729 Filed 3-22-17; 8:45 am]
 BILLING CODE 4410-09-P