2018-23695. Bulk Manufacturer of Controlled Substances Application: Sigma Aldrich Research  

  • Start Preamble Start Printed Page 54613

    ACTION:

    Notice of application.

    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 December 31, 2018.

    ADDRESSES:

    Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152.

    End Preamble Start Supplemental Information

    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 delegated 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 June 14, 2018, Sigma Aldrich Research, 1-3 Strathmore Road, Natick, Massachusetts 01760-2447 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances:

    Controlled substanceDrug codeSchedule
    Cathinone1235I
    Mephedrone (4-Methyl-N-methylcathinone)1248I
    Lysergic acid diethylamide7315I
    3,4-Methylenedioxymethamphetamine7405I
    Dimethyltryptamine7435I
    5-Methoxy-N,N-diisopropyltryptamine7439I
    MDPV (3,4-Methylenedioxypyrovalerone)7535I
    Heroin9200I
    Normorphine9313I
    Norlevorphanol9634I
    Amphetamine1100II
    Nabilone7379II
    Cocaine9041II
    Codeine9050II
    Ecgonine9180II
    Levorphanol9220II
    Meperidine9230II
    Methadone9250II
    Morphine9300II
    Thebaine9333II
    Levo-alphacetylmethadol9648II
    Remifentanil9739II
    Sufentanil9740II
    Carfentanil9743II
    Fentanyl9801II

    The company plans to manufacture reference standards.

    Start Signature

    Dated: October 11, 2018.

    John J. Martin,

    Assistant Administrator.

    End Signature End Supplemental Information

    [FR Doc. 2018-23695 Filed 10-29-18; 8:45 am]

    BILLING CODE 4410-09-P

Document Information

Published:
10/30/2018
Department:
Drug Enforcement Administration
Entry Type:
Notice
Action:
Notice of application.
Document Number:
2018-23695
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 December 31, 2018.
Pages:
54613-54613 (1 pages)
Docket Numbers:
Docket No. DEA-392
PDF File:
2018-23695.pdf