Bulk Manufacturer of Controlled Substances Application: Pisgah Laboratories, Inc., 16654 [2020-06168]
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Federal Register / Vol. 85, No. 57 / Tuesday, March 24, 2020 / Notices
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–607]
Bulk Manufacturer of Controlled
Substances Application: Pisgah
Laboratories, Inc.
ACTION:
Notice of application.
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 May 26, 2020.
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 February 3, 2020,
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
substances:
DATES:
Drug
code
Controlled substance
Difenoxin .......................
Diphenoxylate ...............
Levorphanol ..................
Meperidine intermediate-B.
9168
9170
9220
9233
Schedule
I
II
II
II
The company plans to manufacture
the above-listed controlled substances
in bulk for distribution to its customers.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–06168 Filed 3–23–20; 8:45 am]
BILLING CODE 4410–09–P
hearing on the application on or before
April 23, 2020.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing must
be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All request for a hearing
should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on January 28, 2020, Sharp
(Bethlehem), LLC, 2400 Baglyos Circle,
Bethlehem, Pennsylvania 18020–8024
applied to be registered as an importer
of the following basic class(es) of
controlled substances:
Controlled substance
Gamma Hydroxybutyric
Acid.
3,4-Methylenedioxy
methamphetamine.
Psilocybin .....................
Drug
code
Schedule
2010
I
7405
I
7437
I
The company plans to import the
listed controlled substances for clinical
trials. Approval of permit applications
will occur only when the registrant’s
activity is consistent with what is
authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of FDA-approved or nonapproved finished dosage forms for
commercial sale.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020–06167 Filed 3–23–20; 8:45 am]
DEPARTMENT OF JUSTICE
BILLING CODE 4410–09–P
Drug Enforcement Administration
[Docket No. DEA–605]
DEPARTMENT OF JUSTICE
By order of the Commission.
Issued: March 19, 2020.
Lisa Barton,
Secretary to the Commission.
Importer of Controlled Substances
Application: Sharp (Bethlehem), LLC
Drug Enforcement Administration
[FR Doc. 2020–06152 Filed 3–23–20; 8:45 am]
DATES:
ACTION:
BILLING CODE 7020–02–P
VerDate Sep<11>2014
17:34 Mar 23, 2020
Jkt 250001
Notice of application.
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 April 23, 2020. Such persons
may also file a written request for a
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
[Docket No. DEA–608]
Bulk Manufacturer of Controlled
Substances Application: Cargill, Inc.
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
DATES:
E:\FR\FM\24MRN1.SGM
24MRN1
]]>Agencies
[Federal Register Volume 85, Number 57 (Tuesday, March 24, 2020)]
[Notices]
[Page 16654]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-06168]
=======================================================================
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-607]
Bulk Manufacturer of Controlled Substances Application: Pisgah
Laboratories, Inc.
ACTION: Notice of application.
-----------------------------------------------------------------------
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 May 26, 2020.
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 February 3, 2020, 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 substances:
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Difenoxin.............................. 9168 I
Diphenoxylate.......................... 9170 II
Levorphanol............................ 9220 II
Meperidine intermediate-B.............. 9233 II
------------------------------------------------------------------------
The company plans to manufacture the above-listed controlled
substances in bulk for distribution to its customers.
Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-06168 Filed 3-23-20; 8:45 am]
BILLING CODE 4410-09-P
