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Importer of Controlled Substances Application: Leading Pharma LLC

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Summary

The DEA published notice that Leading Pharma LLC, 3 Oak Road, Fairfield, New Jersey 07004, applied on March 25, 2026 to be registered as an importer of Diphenoxylate (drug code 9170, Schedule II controlled substance). The company plans to import the listed controlled substance as an active pharmaceutical ingredient for research and development toward manufacturing a finished dosage product for Food and Drug Administration approval. Public comments on the application and requests for a hearing must be submitted on or before May 21, 2026.

“The company plans to import the listed controlled substance as an active pharmaceutical ingredient for research and development toward manufacturing a finished dosage product for Food and Drug Administration approval.”

Published by Justice Department on federalregister.gov . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

The DEA published a notice of application by Leading Pharma LLC to be registered as an importer of Diphenoxylate (Schedule II, drug code 9170). The application is for importing the controlled substance as an active pharmaceutical ingredient for research and development toward an FDA-approved finished dosage product. Authorization under this registration will not extend to the import of FDA-approved or non-approved finished dosage forms for commercial sale. Registered bulk manufacturers of the affected controlled substance class and applicants may submit comments or hearing requests through May 21, 2026.

Affected parties include registered bulk manufacturers of Schedule II controlled substances and applicants seeking similar importer registrations. The notice advises that all comments must be submitted electronically through Regulations.gov, and hearing requests must be sent to designated DEA addresses in Springfield, Virginia.

Archived snapshot

Apr 21, 2026

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Notice

Importer of Controlled Substances Application: Leading Pharma LLC

A Notice by the Drug Enforcement Administration on 04/21/2026

  • This document has a comment period that ends in 30 days.
    (05/21/2026) View Comment Instructions

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  • Public Inspection Published Document: 2026-07696 (91 FR 21314) Document Headings ###### Department of Justice
Drug Enforcement Administration
  1. [Docket No. DEA-1706]

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:

Leading Pharma 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 May 21, 2026. Such persons may also file a written request for a hearing on the application on or before May 21, 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 March 25, 2026, Leading Pharma LLC, 3 Oak Road, Fairfield, New Jersey 07004, applied to be registered as an importer of the following basic class(es) of controlled substance(s):

| Controlled substance | Drug
code | Schedule |
| --- | --- | --- |
| Diphenoxylate | 9170 | II |
The company plans to import the listed controlled substance as an active pharmaceutical ingredient for research and development toward manufacturing a finished dosage product for Food and Drug Administration approval. No other activity for this drug code is 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. 2026-07696 Filed 4-20-26; 8:45 am]

BILLING CODE P

Published Document: 2026-07696 (91 FR 21314)

CFR references

21 CFR 1301.34(a)

Citations

21 CFR 1301.34(a) application notice requirements
21 U.S.C. 952 import authorization scope limitation

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Last updated

Classification

Agency
Justice Department
Published
April 21st, 2026
Comment period closes
May 21st, 2026 (30 days)
Compliance deadline
May 21st, 2026 (30 days)
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
91 FR 21314 / Docket No. DEA-1706
Docket
Docket No. DEA-1706

Who this affects

Applies to
Pharmaceutical companies Drug manufacturers Importers and exporters
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Controlled substance import Pharmaceutical R&D DEA registration
Geographic scope
United States US

Taxonomy

Primary area
Pharmaceuticals
Operational domain
Regulatory Affairs
Topics
Healthcare International Trade

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