Notice2022-00326
Bulk Manufacturer of Controlled Substances Application: Johnson Matthey, Inc.
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
January 11, 2022
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
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.
Full Text
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<title>Federal Register, Volume 87 Issue 7 (Tuesday, January 11, 2022)</title>
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[Federal Register Volume 87, Number 7 (Tuesday, January 11, 2022)]
[Notices]
[Page 1435]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2022-00326]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-942]
Bulk Manufacturer of Controlled Substances Application: Johnson
Matthey, Inc.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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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.
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):
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Drug
Controlled Substance Code Schedule
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Gamma Hydroxybutyric Acid............... 2010 I
Marihuana............................... 7360 I
Tetrahydrocannabinols................... 7370 I
Noroxymorphone.......................... 9145 I
Difenoxin............................... 9168 I
Amphetamine............................. 1100 II
Methamphetamine......................... 1105 II
Lisdexamfetamine........................ 1205 II
Methylphenidate......................... 1724 II
Nabilone................................ 7379 II
4-Anilino-N-Phenethyl-4-Piperidine 8333 II
(ANPP).
Norfentanyl............................. 8366 II
Cocaine................................. 9041 II
Codeine................................. 9050 II
Dihydrocodeine.......................... 9120 II
Oxycodone............................... 9143 II
Hydromorphone........................... 9150 II
Diphenoxylate........................... 9170 II
Ecgonine................................ 9180 II
Hydrocodone............................. 9193 II
Levorphanol............................. 9220 II
Meperidine.............................. 9230 II
Methadone............................... 9250 II
Methadone intermediate.................. 9254 II
Morphine................................ 9300 II
Thebaine................................ 9333 II
Opium tincture.......................... 9630 II
Oxymorphone............................. 9652 II
Noroxymorphone.......................... 9668 II
Alfentanil.............................. 9737 II
Remifentanil............................ 9739 II
Sufentanil.............................. 9740 II
Tapentadol.............................. 9780 II
Fentanyl................................ 9801 II
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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.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2022-00326 Filed 1-10-22; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on January 11, 2022.
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