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Notice

Bulk Manufacturer of Controlled Substances Application: Navinta LLC

Notice of application.

📖 Research Context From Federal Register API

Summary:

Navinta 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.

Key Dates
Citation: 90 FR 59871
Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on or objections to the issuance of the prosed registration on or before February 20, 2026. Such persons may also file a written request for a hearing on the application on or before February 20, 2026.
Comments close: February 20, 2026
Public Participation

In Plain English

What is this Federal Register notice?

This is a notice published in the Federal Register by Justice Department, Drug Enforcement Administration. Notices communicate information, guidance, or policy interpretations but may not create new binding obligations.

Is this rule final?

This document is classified as a notice. It may or may not create enforceable regulatory obligations depending on its specific content.

Who does this apply to?

Notice of application.

When does it take effect?

Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on or objections to the issuance of the prosed registration on or before February 20, 2026. Such persons may also file a written request for a hearing on the application on or before February 20, 2026.

Why it matters: This notice communicates agency policy or guidance regarding applicable regulations.

Document Details

Document Number2025-23620
FR Citation90 FR 59871
TypeNotice
PublishedDec 22, 2025
Effective Date-
RIN-
Docket IDDocket No. DEA-1636
Pages59871–59872 (2 pages)
Text FetchedYes

Agencies & CFR References

CFR References:
None

Linked CFR Parts

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📋 Extracted Requirements 0 found

No extractable regulatory requirements found in this document. This is common for documents that:

  • Incorporate requirements by reference (IBR) to external documents
  • Are procedural notices without substantive obligations
  • Contain only preamble/explanation without regulatory text

Full Document Text (330 words · ~2 min read)

Text Preserved
<NOTICE> DEPARTMENT OF JUSTICE <SUBAGY>Drug Enforcement Administration</SUBAGY> <DEPDOC>[Docket No. DEA-1636]</DEPDOC> <SUBJECT>Bulk Manufacturer of Controlled Substances Application: Navinta LLC</SUBJECT> <HD SOURCE="HED">AGENCY:</HD> Drug Enforcement Administration, Justice. <HD SOURCE="HED">ACTION:</HD> Notice of application. <SUM> <HD SOURCE="HED">SUMMARY:</HD> Navinta LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to <E T="02">SUPPLEMENTARY INFORMATION</E> listed below for further drug information. </SUM> <DATES> <HD SOURCE="HED">DATES:</HD> Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on or objections to the issuance of the prosed registration on or before February 20, 2026. Such persons may also file a written request for a hearing on the application on or before February 20, 2026. </DATES> <HD SOURCE="HED">ADDRESSES:</HD> 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 <E T="03">https://www.regulations.gov</E> 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 <E T="03">https://www.regulations.gov.</E> If you have received a Comment Tracking Number, your comment has been successfully submitted and there is no need to resubmit the same comment. <SUPLINF> <HD SOURCE="HED">SUPPLEMENTARY INFORMATION:</HD> In accordance with <E T="03">21 CFR 1301.33(a),</E> this is notice that on October 16, 2025, Navinta LLC, 1499 Lower Ferry Road, Ewing, New Jersey 08618-1414, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): <GPOTABLE COLS="3" OPTS="L2,nj,tp0,i1" CDEF="s25,6,xls36"> <TTITLE> </TTITLE> <CHED H="1">Controlled substance</CHED> <CHED H="1"> Drug code </CHED> <CHED H="1">Schedule</CHED> The company plans to bulk manufacture the listed controlled substance for distribution to their customers. No other activity for this drug code is authorized for this registration. <SIG> <NAME>Thomas Prevoznik,</NAME> Deputy Assistant Administrator. </SIG> </SUPLINF> <FRDOC>[FR Doc. 2025-23620 Filed 12-19-25; 8:45 am]</FRDOC> </NOTICE>
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