90 FR 29 pgs. 9554-9555 - Importer of Controlled Substances Application: Purisys, LLC
Type: NOTICEVolume: 90Number: 29Pages: 9554 - 9555
Pages: 9554, 9555Docket number: [Docket No. DEA-1491]
FR document: [FR Doc. 2025-02600 Filed 2-12-25; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version: PDF Version
[top]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1491]
Importer of Controlled Substances Application: Purisys, LLC
AGENCY:
Drug Enforcement Administration, Justice.
ACTION:
Notice of application.
SUMMARY:
Purisys, LLC has applied to be registered as an importer 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 March 17, 2025. Such persons may also file a written request for a hearing on the application on or before March 17, 2025.
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. All requests for a hearing must 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. All requests for a hearing should also be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION:
[top] In accordance with 21 CFR 1301.34(a), this is notice that on December 10, 2024, Purisys, LLC, 1550 Olympic Drive, Athens, Georgia 30601-1602, applied to be registered as an importer of the following basic class(es) of controlled substance(s):
| Controlled substance | Drug code | Schedule |
|---|---|---|
| Marihuana Extract | 7350 | I |
| Marihuana | 7360 | I |
| Tetrahydrocannabinols | 7370 | I |
| Nabilone | 7379 | II |
| Phenylacetone | 8501 | II |
| Ecgonine | 9180 | II |
| Levorphanol | 9220 | II |
| Methadone | 9250 | II |
| Thebaine | 9333 | II |
| Opium, raw | 9600 | II |
| Opium, powdered | 9639 | II |
| Opium, granulated | 9640 | II |
| Noroxymorphone | 9668 | II |
| Poppy Straw Concentrate | 9670 | II |
| Tapentadol | 9780 | II |
The company plans to import Opium, Raw (9600), Opium, Powdered (9639) and Opium, Granulated (9640) to manufacture an Active Pharmaceutical Ingredient (API) only for distribution to its customers. The company plans to import Phenylacetone (8501) and Poppy Straw Concentrate (9670), to bulk manufacture other controlled substances for distribution to its customers. The company plans to import impurities of buprenorphine that have been determined by DEA to be captured under Thebaine (9333). In reference to Marihuana Extract (7350), Marihuana (7360), and Tetrahydrocannabinols (7370), the company plans to import as synthetic. The company plans to import an isomer of methadone (9250) not currently available domestically to manufacture a non-controlled substance. No other activities for these drug codes are authorized for this registration.
Approval of permit applications will occur only when the registrant's business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Authorization will not extend to the import of Food and Drug Administration-approved or non-approved finished dosage forms for commercial sale.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-02600 Filed 2-12-25; 8:45 am]
BILLING CODE P