[Federal Register Volume 85, Number 103 (Thursday, May 28, 2020)]
[Notices]
[Page 32050]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-11393]



[[Page 32050]]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-650]


Importer of Controlled Substances Application: Rhodes 
Technologies

ACTION: Notice of application.

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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 June 29, 2020. 
Such persons may also file a written request for a hearing on the 
application on or before June 29, 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 
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: In accordance with 21 CFR 1301.34(a), this 
is notice that on February 13, 2020, Rhodes Technologies, 498 
Washington Street, Coventry, Rhode Island 02816, applied to be 
registered as an importer of the following basic class(es) of 
controlled substances:

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          Controlled substance               Drug code       Schedule
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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
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    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.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-11393 Filed 5-27-20; 8:45 am]
BILLING CODE 4410-09-P