Notice2021-25578
Bulk Manufacturer of Controlled Substances Application: Noramco
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
November 23, 2021
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Noramco, has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Full Text
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<title>Federal Register, Volume 86 Issue 223 (Tuesday, November 23, 2021)</title>
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[Federal Register Volume 86, Number 223 (Tuesday, November 23, 2021)]
[Notices]
[Page 66589]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2021-25578]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-925]
Bulk Manufacturer of Controlled Substances Application: Noramco
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Noramco, has applied to be registered as a bulk manufacturer
of basic class(es) of controlled substance(s). Refer to Supplementary
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 January 24,
2022. Such persons may also file a written request for a hearing on the
application on or before January 24, 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 October 19, 2021, Noramco, 500 Swedes Landing Road,
Wilmington, Delaware 19801-4417, 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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Marihuana............................... 7360 I
Tetrahydrocannabinols................... 7370 I
Dihydromorphine......................... 9145 I
Hydromorphinol.......................... 9301 I
Amphetamine............................. 1100 II
Lisdexamfetamine........................ 1205 II
Methylphenidate......................... 1724 II
Nabilone................................ 7379 II
Codeine................................. 9050 II
Dihydrocodeine.......................... 9120 II
Oxycodone............................... 9143 II
Hydromorphone........................... 9150 II
Hydrocodone............................. 9193 II
Morphine................................ 9300 II
Oripavine............................... 9330 II
Thebaine................................ 9333 II
Opium extracts.......................... 9610 II
Opium fluid extract..................... 9620 II
Opium, tincture......................... 9630 II
Opium, powdered......................... 9639 II
Opium, granulated....................... 9640 II
Oxymorphone............................. 9652 II
Noroxymorphone.......................... 9668 II
Tapentadol.............................. 9780 II
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The company plans to bulk manufacture the listed controlled
substances as an Active Pharmaceutical Ingredient (API) for supply to
its customers. In reference to dug codes 7360 (Marihuana), and 7370
(Tetrahydrocannabinols), the company plans to bulk manufacture these
drugs as synthetic. No other activities for these drug codes are
authorized for this registration.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-25578 Filed 11-22-21; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on November 23, 2021.
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