[Federal Register Volume 83, Number 28 (Friday, February 9, 2018)]
[Notices]
[Page 5812]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-02642]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Siemens 
Healthcare Diagnostics 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 on or before April 10, 2018.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: 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 1301.33(a), this is notice that on 
December 13, 2017, Siemens Healthcare Diagnostics Inc., 100 GBC Drive, 
Mailstop 514, Newark, DE 19702 applied to be registered as a bulk 
manufacturer of the following basic class of controlled substance:

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                                           Drug
          Controlled substance             code          Schedule
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Ecgonine...............................     9180  II
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    The company plans to bulk manufacture a material used in the 
manufacture of reagents for a Cocaine in vitro diagnostic test system.

    Dated: February 1, 2018.
 Susan A. Gibson,
 Deputy Assistant Administrator.
[FR Doc. 2018-02642 Filed 2-8-18; 8:45 am]
 BILLING CODE 4410-09-P