[Federal Register Volume 89, Number 58 (Monday, March 25, 2024)]
[Notices]
[Pages 20699-20700]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-06193]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1346]


Bulk Manufacturer of Controlled Substances Application: Restek 
Corporation

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Restek Corporation has applied to be registered as a bulk 
manufacturer of basic class(es) of controlled substance(s). Refer to 
SUPPLEMENTARY INFORMATION listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may submit electronic comments on or 
objections to the issuance of the proposed registration on or before 
May 24, 2024. Such persons may also file a written request for a 
hearing on the application on or before May 24, 2024.

ADDRESSES: The Drug Enforcement Administration requires that all 
comments be submitted electronically through the Federal eRulemaking 
Portal, which provides the ability to type short comments directly into 
the comment field on the web page or attach a file for lengthier 
comments. Please go to https://www.regulations.gov and follow the 
online instructions at that site for submitting comments. Upon 
submission of your comment, you will receive a Comment Tracking Number. 
Please be aware that submitted comments are not instantaneously 
available for public view on https://www.regulations.gov. If you have 
received a Comment Tracking Number, your comment has been successfully 
submitted and there is no need to resubmit the same comment.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on January 31, 2024, Restek Corporation, 110 Benner 
Circle, Bellefonte, Pennsylvania 16823-8433 applied to be registered as 
a bulk manufacturer of the following basic class(es) of controlled 
substance(s):

[[Page 20700]]



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            Controlled substance              Drug code      Schedule
------------------------------------------------------------------------
Gamma Hydroxybutyric Acid..................        2010  I
Methaqualone...............................        2565  I
JWH-018 (also known as AM678) (1-Pentyl-3-         7118  I
 (1-naphthoyl)indole).
JWH-200 (1-[2-(4-Morpholinyl)ethyl]-3-(1-          7200  I
 naphthoyl)indole).
CP-47,497 (5-(1,1-Dimethylheptyl)-2-               7297  I
 [(1R,3S)-3-hydroxycyclohexyl-phenol).
CP-47,497 C8 Homologue (5-(1,1-                    7298  I
 Dimethyloctyl)-2-[(1R,3S)3-
 hydroxycyclohexyl-phenol).
Lysergic acid diethylamide.................        7315  I
Marihuana..................................        7360  I
Tetrahydrocannabinols......................        7370  I
4-Methyl-2,5-dimethoxyamphetamine..........        7395  I
3,4-Methylenedioxyamphetamine..............        7400  I
3,4-Methylenedioxy-N-ethylamphetamine......        7404  I
3,4-Methylenedioxymethamphetamine..........        7405  I
Bufotenine.................................        7433  I
Psilocybin.................................        7437  I
Psilocyn...................................        7438  I
Cyprenorphine..............................        9054  I
Dihydromorphine............................        9145  I
Heroin.....................................        9200  I
Normorphine................................        9313  I
Beta-hydroxyfentanyl.......................        9830  I
Beta-hydroxy-3-methylfentanyl..............        9831  I
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances for the Drug Enforcement Administration-exempted certified 
reference materials. In-house synthesis gives access to compounds that 
are difficult to source. In reference to drug codes 7360 (Marihuana), 
and 7370 (Tetrahydrocannabinols), the company plans to bulk manufacture 
these drugs as synthetic. No other activities for these drug codes are 
authorized for this registration.

Marsha Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-06193 Filed 3-22-24; 8:45 am]
BILLING CODE P