Notice2021-25950
Bulk Manufacturer of Controlled Substances Application: Patheon API Manufacturing, 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
November 29, 2021
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Patheon API Manufacturing, 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 86 Issue 226 (Monday, November 29, 2021)</title>
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[Federal Register Volume 86, Number 226 (Monday, November 29, 2021)]
[Notices]
[Page 67725]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2021-25950]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-930]
Bulk Manufacturer of Controlled Substances Application: Patheon
API Manufacturing, Inc.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Patheon API Manufacturing, 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 January 28,
2022. Such persons may also file a written request for a hearing on the
application on or before January 28, 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 3, 2021, Patheon API Manufacturing, Inc.,
309 Delaware Street, Greenville, South Carolina 29605-5420, 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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Dimethyltryptamine.................................. 7435 I
Psilocyn............................................ 7438 I
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The company plans to bulk manufacture the listed controlled
substances as an Active Pharmaceutical Ingredient (API) for
distribution to its customers. No other activities for these drug codes
are authorized for this registration.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-25950 Filed 11-26-21; 8:45 am]
BILLING CODE P
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</html>Indexed from Federal Register on November 29, 2021.
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