2022-00326. Bulk Manufacturer of Controlled Substances Application: Johnson Matthey, Inc.  

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    AGENCY:

    Drug Enforcement Administration, Justice.

    ACTION:

    Notice of application.

    SUMMARY:

    Johnson Matthey, Inc., has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.

    DATES:

    Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before March 14, 2022. Such persons may also file a written request for a hearing on the application on or before March 14, 2022.

    ADDRESSES:

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

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    SUPPLEMENTARY INFORMATION:

    In accordance with 21 CFR 1301.33(a), this is notice that on November 2, 2021, Johnson Matthey, Inc., 2003 Nolte Drive West Deptford, New Jersey 08066-1742, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s):

    Controlled SubstanceDrug CodeSchedule
    Gamma Hydroxybutyric Acid2010I
    Marihuana7360I
    Tetrahydrocannabinols7370I
    Noroxymorphone9145I
    Difenoxin9168I
    Amphetamine1100II
    Methamphetamine1105II
    Lisdexamfetamine1205II
    Methylphenidate1724II
    Nabilone7379II
    4-Anilino-N-Phenethyl-4-Piperidine (ANPP)8333II
    Norfentanyl8366II
    Cocaine9041II
    Codeine9050II
    Dihydrocodeine9120II
    Oxycodone9143II
    Hydromorphone9150II
    Diphenoxylate9170II
    Ecgonine9180II
    Hydrocodone9193II
    Levorphanol9220II
    Meperidine9230II
    Methadone9250II
    Methadone intermediate9254II
    Morphine9300II
    Thebaine9333II
    Opium tincture9630II
    Oxymorphone9652II
    Noroxymorphone9668II
    Alfentanil9737II
    Remifentanil9739II
    Sufentanil9740II
    Tapentadol9780II
    Fentanyl9801II

    The company plans to bulk manufacture the listed controlled substances for the internal use intermediates or for sale to its customers. In reference to drug codes 7360 (Marihuana), and 7370 (Tetrahydrocannabinols), the company plans to bulk manufacture these drugs as synthetic. The company plans to bulk manufacture for either internal usage as intermediates or to sale to customers as Active Pharmaceutical Ingredients (API). No other activities for these drug codes are authorized for this registration.

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    Brian S. Besser,

    Acting Assistant Administrator.

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    [FR Doc. 2022-00326 Filed 1-10-22; 8:45 am]

    BILLING CODE P

Document Information

Published:
01/11/2022
Department:
Drug Enforcement Administration
Entry Type:
Notice
Action:
Notice of application.
Document Number:
2022-00326
Dates:
Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before March 14, 2022. Such persons may also file a written request for a hearing on the application on or before March 14, 2022.
Pages:
1435-1435 (1 pages)
Docket Numbers:
Docket No. DEA-942
PDF File:
2022-00326.pdf