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DEA Notice: SpecGx LLC Controlled Substances Importer Application

Favicon for www.federalregister.gov FR: Drug Enforcement Administration
Published March 19th, 2026
Detected March 19th, 2026
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Summary

The Drug Enforcement Administration (DEA) has published a notice regarding an application from SpecGx LLC to be registered as an importer of controlled substances, including Phenylacetone, Coca Leaves, Thebaine, Opium, Poppy Straw Concentrate, and Tapentadol. Interested parties can submit comments or objections by April 20, 2026.

What changed

The Drug Enforcement Administration (DEA) has issued a notice concerning an application filed by SpecGx LLC for registration as an importer of specific controlled substances, including Phenylacetone, Coca Leaves, Thebaine, Opium, Poppy Straw Concentrate, and Tapentadol. These substances are classified under Schedule II. SpecGx LLC intends to import these controlled substances for the bulk manufacture of Active Pharmaceutical Ingredients.

Registered bulk manufacturers and other interested parties have until April 20, 2026, to submit electronic comments or objections to the proposed registration, or to file a written request for a hearing. The DEA requires electronic submissions through the Federal eRulemaking Portal. Failure to act by the deadline may result in the approval of the application without further notice.

What to do next

  1. Review SpecGx LLC's application for controlled substances importation.
  2. Submit electronic comments or objections by April 20, 2026, if applicable.
  3. File a written request for a hearing by April 20, 2026, if applicable.

Source document (simplified)

Notice

Importer of Controlled Substances Application: SpecGx LLC

A Notice by the Drug Enforcement Administration on 03/19/2026

  • This document has a comment period that ends in 32 days.
    (04/20/2026) View Comment Instructions

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  • Public Inspection Published Document: 2026-05353 (91 FR 13336) Document Headings ###### Department of Justice
Drug Enforcement Administration
  1. [Docket No. DEA-1683]

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:

SpecGx 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 April 20, 2026. Such persons may also file a written request for a hearing on the application on or before April 20, 2026.

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:

In accordance with 21 CFR 1301.34(a), this is notice that on February 3, 2026, SpecGx LLC, 3600 North 2nd Street, Saint Louis, Missouri 63147-3457, applied to be registered as an importer of the following basic class(es) of controlled substance(s):

| Controlled
substance | Drug
code | Schedule |
| --- | --- | --- |
| Phenylacetone | 8501 | II |
| Coca Leaves | 9040 | II |
| Thebaine | 9333 | II |
| Opium, raw | 9600 | II |
| Poppy Straw Concentrate | 9670 | II |
| Tapentadol | 9780 | II |
The company plans to import the listed controlled substances for bulk manufacture into Active Pharmaceutical Ingredients for distribution to its customers. In reference to Tapentadol (9780) and Thebaine (9333), the company plans to import intermediate forms of these controlled substances for further manufacturing prior to distribution to its customers. 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.

Thomas Prevoznik,

Deputy Assistant Administrator.

[FR Doc. 2026-05353 Filed 3-18-26; 8:45 am]

BILLING CODE 4410-09-P

Published Document: 2026-05353 (91 FR 13336)

Classification

Agency
DEA
Published
March 19th, 2026
Compliance deadline
April 20th, 2026 (32 days)
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Drug manufacturers
Geographic scope
National (US) National (US)

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Compliance
Topics
Controlled Substances Drug Manufacturing Import/Export

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