87 FR 67 pg. 20464 - Bulk Manufacturer of Controlled Substances Application: Purisys, LLC

Type: NOTICEVolume: 87Number: 67Page: 20464
Docket number: [Docket No. DEA-988]
FR document: [FR Doc. 2022-07368 Filed 4-6-22; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version:  PDF Version
Page: 20464

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-988]

Bulk Manufacturer of Controlled Substances Application: Purisys, LLC

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:

Purisys, LLC. 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 June 6, 2022. Such persons may also file a written request for a hearing on the application on or before June 6, 2022.

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 21, 2022, 1550 Olympic Drive, Athens, Georgia 30601-1602, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s):

Controlled substance Drug code Schedule
Cathinone 1235 I
Gamma Hydroxybutyric Acid 2010 I
Lysergic acid diethylamide 7315 I
Marihuana Extract 7350 I
Marihuana 7360 I
Tetrahydrocannabinols 7370 I
2,5-Dimethoxyamphetamine 7396 I
3,4-Methylenedioxy amphetamine. 7400 I
5-Methoxy-3,4-methylenedioxy amphetamine 7401 I
3,4-Methylenedioxy methamphetamine. 7405 I
5-Methoxy-N-N-dimethyl tryptamine. 7431 I
Diethyltryptamine 7434 I
Dimethyltryptamine 7435 I
Psilocybin 7437 I
Psilocyn 7438 I
Codeine-N-oxide 9053 I
Dihydromorphine 9145 I
Hydromorphinol 9301 I
Morphine-N-oxide 9307 I
Normorphine 9313 I
Norlevorphanol 9634 I
Codeine 9050 II
Dihydrocodeine 9120 II
Oxycodone 9143 II
Hydromorphone 9150 II
Hydrocodone 9193 II
Levorphanol 9220 II
Morphine 9300 II
Oripavine 9330 II
Thebaine 9333 II
Opium tincture 9630 II
Opium, powdered 9639 II
Opium, granulated 9640 II
Oxymorphone 9652 II
Noroxymorphone 9668 II
Alfentanil 9737 II
Sufentanil 9740 II
Carfentanil 9743 II
Tapentadol 9780 II
Fentanyl 9801 II

The company plans to bulk manufacture the listed controlled substances for internal use intermediates or for sale to its customers. The company plans to manufacture the above-listed controlled substances as clinical trial and starting materials to make compounds for distribution to its customers. No other activities for these drug codes are authorized for this registration.

Matthew J. Strait,

Deputy Assistant Administrator.

[FR Doc. 2022-07368 Filed 4-6-22; 8:45 am]

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