Importer of Controlled Substances Application: Rhodes Technologies, 21807 [2019-10010]
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Federal Register / Vol. 84, No. 94 / Wednesday, May 15, 2019 / Notices
transfer of control of the cultural item to
the lineal descendants, Indian Tribes, or
Native Hawaiian organizations stated in
this notice may proceed.
DATES: Lineal descendants or
representatives of any Indian Tribe or
Native Hawaiian organization not
identified in this notice that wish to
claim this cultural item should submit
a written request with information in
support of the claim to the Pueblo
Grande Museum at the address in this
notice by June 14, 2019.
ADDRESSES: Lindsey Vogel-Teeter,
Pueblo Grande Museum, 4619 E
Washington Street, Phoenix, AZ 85331,
telephone (602) 495–0901, email
lindsey.vogel-teeter@phoenix.gov.
SUPPLEMENTARY INFORMATION: Notice is
here given in accordance with the
Native American Graves Protection and
Repatriation Act (NAGPRA), 25 U.S.C.
3005, of the intent to repatriate a
cultural item under the control of the
Pueblo Grande Museum, Phoenix, AZ,
that meets the definition of a sacred
object under 25 U.S.C. 3001.
This notice is published as part of the
National Park Service’s administrative
responsibilities under NAGPRA, 25
U.S.C. 3003(d)(3). The determinations in
this notice are the sole responsibility of
the museum, institution, or Federal
agency that has control of the Native
American cultural item. The National
Park Service is not responsible for the
determinations in this notice.
History and Description of the Cultural
Item
Around 1983, a Butterfly Dance
Tablita (headdress) was donated to the
Pueblo Grande Museum by Holley
Swan, a patron of the Museum. No
additional information is known about
the collecting history of this object.
During consultation on January 10,
2017, representatives of the Hopi Tribe
of Arizona demonstrated the Tribe’s
cultural affiliation with this object, and
established that the object was needed
for use by girls during a traditional Hopi
ceremony, the Butterfly dance.
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Determinations Made by the Pueblo
Grande Museum
Officials of the Pueblo Grande
Museum have determined that:
• Pursuant to 25 U.S.C. 3001(3)(C),
the one cultural item described above is
a specific ceremonial object needed by
traditional Native American religious
leaders for the practice of traditional
Native American religions by their
present-day adherents.
• Pursuant to 25 U.S.C. 3001(2), there
is a relationship of shared group
identity that can be reasonably traced
VerDate Sep<11>2014
22:43 May 14, 2019
Jkt 247001
between the sacred object and the Hopi
Tribe of Arizona.
Additional Requestors and Disposition
Lineal descendants or representatives
of any Indian Tribe or Native Hawaiian
organization not identified in this notice
that wish to claim this cultural item
should submit a written request with
information in support of the claim to
Lindsey Vogel-Teeter, Pueblo Grande
Museum, 4619 E Washington Street,
Phoenix, AZ 85331, telephone (602)
495–0901, email lindsey.vogel-teeter@
phoenix.gov, by June 14, 2019. After
that date, if no additional claimants
have come forward, transfer of control
of the sacred object to the Hopi Tribe of
Arizona may proceed.
The Pueblo Grande Museum is
responsible for notifying the Hopi Tribe
of Arizona that this notice has been
published.
Dated: April 25, 2019.
Melanie O’Brien,
Manager, National NAGPRA Program.
[FR Doc. 2019–09995 Filed 5–14–19; 8:45 am]
BILLING CODE 4312–52–P
The
Attorney General has delegated his
authority under the Controlled
Substances Act to the Administrator of
the Drug Enforcement Administration
(DEA), 28 CFR 0.100(b). Authority to
exercise all necessary functions with
respect to the promulgation and
implementation of 21 CFR part 1301,
incident to the registration of
manufacturers, distributors, dispensers,
importers, and exporters of controlled
substances (other than final orders in
connection with suspension, denial, or
revocation of registration) has been
redelegated to the Assistant
Administrator of the DEA Diversion
Control Division (‘‘Assistant
Administrator’’) pursuant to section 7 of
28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR
1301.34(a), this is notice that on March
11, 2019, Rhodes Technologies, 498
Washington Street, Coventry, Rhode
Island 02816 applied to be registered as
an importer of the following basic
classes of controlled substances:
SUPPLEMENTARY INFORMATION:
Controlled substance
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–392]
Importer of Controlled Substances
Application: Rhodes Technologies
ACTION:
Notice of application.
Registered bulk manufacturers of
the affected basic classes, and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before June 14, 2019. Such persons
may also file a written request for a
hearing on the application on or before
June 14, 2019.
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 requests 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.
DATES:
PO 00000
Frm 00060
Fmt 4703
Sfmt 9990
Tetrahydrocannabinols ..
Methylphenidate .............
Oxycodone .....................
Hydromorphone .............
Hydrocodone ..................
Morphine ........................
Opium, raw ....................
Oxymorphone ................
Poppy Straw Concentrate.
Drug code
7370
1724
9143
9150
9193
9300
9600
9652
9670
Schedule
I
II
II
II
II
II
II
II
II
The company plans to import Opium,
raw (9600), and Poppy Straw
Concentrate (9670) in order to bulk
manufacture controlled substances in
Active Pharmaceutical Ingredient (API)
form. The company distributes the
manufactured APIs in bulk to its
customers.
The company plans to import the
other listed controlled substances for
internal reference standards use only.
The comparisons of foreign reference
standards to the company’s
domestically manufactured API will
allow the company to export
domestically manufactured API to
foreign markets.
Dated: April 27, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019–10010 Filed 5–14–19; 8:45 am]
BILLING CODE 4410–09–P
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]]>Agencies
[Federal Register Volume 84, Number 94 (Wednesday, May 15, 2019)]
[Notices]
[Page 21807]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-10010]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-392]
Importer of Controlled Substances Application: Rhodes
Technologies
ACTION: Notice of application.
-----------------------------------------------------------------------
DATES: Registered bulk manufacturers of the affected basic classes, and
applicants therefore, may file written comments on or objections to the
issuance of the proposed registration on or before June 14, 2019. Such
persons may also file a written request for a hearing on the
application on or before June 14, 2019.
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
requests 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: The Attorney General has delegated his
authority under the Controlled Substances Act to the Administrator of
the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority
to exercise all necessary functions with respect to the promulgation
and implementation of 21 CFR part 1301, incident to the registration of
manufacturers, distributors, dispensers, importers, and exporters of
controlled substances (other than final orders in connection with
suspension, denial, or revocation of registration) has been redelegated
to the Assistant Administrator of the DEA Diversion Control Division
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0,
appendix to subpart R.
In accordance with 21 CFR 1301.34(a), this is notice that on March
11, 2019, Rhodes Technologies, 498 Washington Street, Coventry, Rhode
Island 02816 applied to be registered as an importer of the following
basic classes of controlled substances:
------------------------------------------------------------------------
Controlled substance Drug code Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols................ 7370 I
Methylphenidate...................... 1724 II
Oxycodone............................ 9143 II
Hydromorphone........................ 9150 II
Hydrocodone.......................... 9193 II
Morphine............................. 9300 II
Opium, raw........................... 9600 II
Oxymorphone.......................... 9652 II
Poppy Straw Concentrate.............. 9670 II
------------------------------------------------------------------------
The company plans to import Opium, raw (9600), and Poppy Straw
Concentrate (9670) in order to bulk manufacture controlled substances
in Active Pharmaceutical Ingredient (API) form. The company distributes
the manufactured APIs in bulk to its customers.
The company plans to import the other listed controlled substances
for internal reference standards use only. The comparisons of foreign
reference standards to the company's domestically manufactured API will
allow the company to export domestically manufactured API to foreign
markets.
Dated: April 27, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-10010 Filed 5-14-19; 8:45 am]
BILLING CODE 4410-09-P
