Notice2021-25949
Bulk Manufacturer of Controlled Substances Application: Pisgah Laboratories 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
Pisgah Laboratories 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: 2021-25949]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-929]
Bulk Manufacturer of Controlled Substances Application: Pisgah
Laboratories Inc.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Pisgah Laboratories 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 March 30, 2021, Pisgah Laboratories Inc., 3222 Old
Hendersonville Highway, Pisgah Forest, North Carolina 28768, 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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Difenoxin.............................. 9168 I
Methylphenidate........................ 1724 II
Diphenoxylate.......................... 9170 II
Levorphanol............................ 9220 II
Remifentanil........................... 9739 II
Tapentadol............................. 9780 II
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The company plans to manufacture the above-listed controlled
substances in bulk 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. 2021-25949 Filed 11-26-21; 8:45 am]
BILLING CODE 4410-09-P
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</html>Indexed from Federal Register on November 29, 2021.
This is legal information, not legal advice. Laws vary by jurisdiction and change frequently. Always verify current law with official sources and consult a licensed attorney in your jurisdiction for advice on your specific situation.