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Bulk Manufacturer of Controlled Substances Application: Sterling Pharma USA LLC

---
identifier: "/us/fr/2025-04284"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Bulk Manufacturer of Controlled Substances Application: Sterling Pharma USA LLC"
title_number: 0
title_name: "Federal Register"
section_number: "2025-04284"
section_name: "Bulk Manufacturer of Controlled Substances Application: Sterling Pharma USA LLC"
positive_law: false
currency: "2025-03-17"
last_updated: "2025-03-17"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Justice Department"
document_number: "2025-04284"
document_type: "notice"
publication_date: "2025-03-17"
agencies:
  - "Justice Department"
  - "Drug Enforcement Administration"
fr_citation: "90 FR 12367"
fr_volume: 90
docket_ids:
  - "Docket No. DEA-1510"
comments_close_date: "2025-05-16"
fr_action: "Notice of application."
---

#  Bulk Manufacturer of Controlled Substances Application: Sterling Pharma USA LLC

**AGENCY:**

Drug Enforcement Administration, Justice.

**ACTION:**

Notice of application.

**SUMMARY:**

Sterling Pharma USA LLC 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 16, 2025. Such persons may also file a written request for a hearing on the application on or before May 16, 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.

**SUPPLEMENTARY INFORMATION:**

In accordance with 21 CFR 1301.33(a), this is notice that on February 11, 2025, Sterling Pharma USA LLC, 1001 Sheldon Drive, Suite 101, Cary, North Carolina 27513-2078 applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s):

| Controlled substance | Drug code | Schedule |
| --- | --- | --- |
| Tetrahydrocannabinols | 7370 | I |
| 5-Methoxy-N-N-dimethyltryptamine | 7431 | I |
| Dimethyltryptamine | 7435 | I |
| Psilocybin | 7437 | I |
| Psilocyn | 7438 | I |

The company plans to bulk manufacture the listed controlled substance(s) to support internal research and for sale to its customers for pre-clinical trial studies. No other activities for these drug codes are authorized for this registration.

Matthew Strait,

Deputy Assistant Administrator.