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Notice2026-19698

Foreign-Trade Zone (FTZ) 93, Notification of Proposed Production Activity; Eli Lilly and Company; (Drug Products); Durham, North Carolina

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Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
September 25, 2026

Issuing agencies

Commerce DepartmentForeign-Trade Zones Board

Full Text

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<title>Federal Register, Volume 91 Issue 185 (Friday, September 25, 2026)</title>
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[Federal Register Volume 91, Number 185 (Friday, September 25, 2026)]
[Notices]
[Pages 60934-60935]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-19698]


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DEPARTMENT OF COMMERCE

Foreign-Trade Zones Board

[B-122-2026]


Foreign-Trade Zone (FTZ) 93, Notification of Proposed Production 
Activity; Eli Lilly and Company; (Drug Products); Durham, North 
Carolina

    Eli Lilly and Company submitted a notification of proposed 
production activity to the FTZ Board (the Board) for its facility in 
Durham, North Carolina within Subzone 93K. The notification conforming 
to the requirements of the Board's regulations (15 CFR 400.22) was 
received on September 17, 2026.
    Pursuant to 15 CFR 400.14(b), FTZ production activity would be 
limited to the specific foreign-status material(s)/component(s) and 
specific finished product(s) described in the submitted notification 
(summarized below) and subsequently authorized by the Board. The 
benefits that may stem from conducting production activity under FTZ 
procedures are explained in the background section of the Board's 
website--accessible via <a href="http://www.trade.gov/ftz">www.trade.gov/ftz</a>.
    The proposed finished products include: Incretin-based therapy for 
blood glucose and weight management drug product in dosage/packaged 
form in filled syringes, vials, or delivery pens or semi-finished 
syringes; CGRP monoclonal antibody for migraine prevention drug product 
in dosage/packaged form in filled syringes, vials, or delivery pens or 
semi finished syringes; IL-17A monoclonal antibody for chronic 
inflammatory conditions drug product in dosage/packaged form in filled 
syringes, vials, or delivery pens or semi-finished syringes; Incretin-
based therapy for blood glucose management in type 2 diabetes drug 
product in dosage/packaged form in filled syringes, vials, or delivery 
pens or semi-finished syringes; Multi-incretin therapy for weight and 
metabolic management drug product in dosage/packaged form in filled 
syringes, vials, or delivery pens or semi-finished syringes; IL-13-
targeted therapy for atopic dermatitis management drug product in 
dosage/packaged form in filled syringes, vials, or delivery pens or 
semi finished syringes; IL-23-targeted therapy for inflammatory bowel 
disease management drug product in dosage/packaged form in filled 
syringes, vials, or delivery pens or semi-finished syringes; Amylin 
receptor-targeted therapy for weight management drug product in dosage/
packaged form in filled syringes, vials, or delivery pens or semi-
finished syringes; and Amyloid-

[[Page 60935]]

targeted therapy for early Alzheimer's disease drug product in dosage/
packaged form in filled syringes, vials, or delivery pens or semi-
finished syringes (duty free).
    The proposed foreign-status materials/components include: Incretin-
based therapy for blood glucose and weight management drug substance; 
Incretin-based therapy for blood glucose and weight management drug 
product in vials or semi-finished syringes; CGRP monoclonal antibody 
for migraine prevention drug substance; CGRP monoclonal antibody for 
migraine prevention drug product in vials or semi-finished syringes; 
IL-17A monoclonal antibody for chronic inflammatory conditions drug 
substance; IL-17A monoclonal antibody for chronic inflammatory 
conditions drug product in vials or semi-finished syringes; Incretin-
based therapy for blood glucose management in type 2 diabetes drug 
substance; Incretin-based therapy for blood glucose management in type 
2 diabetes drug product in vials or semi-finished syringes; Multi-
incretin therapy for weight and metabolic management drug substance; 
Multi-incretin therapy for weight and metabolic management drug product 
in vials or semi-finished syringes; IL-13-targeted therapy for atopic 
dermatitis management drug substance; IL-13-targeted therapy for atopic 
dermatitis management drug product in vials or semi-finished syringes; 
IL-23-targeted therapy for inflammatory bowel disease management drug 
substance; IL-23-targeted therapy for inflammatory bowel disease 
management drug product in vials or semi-finished syringes; Amylin 
receptor-targeted therapy for weight management drug product in vials 
or semi-finished syringes; Amylin receptor-targeted therapy for weight 
management drug substance; Amyloid-targeted therapy for early 
Alzheimer's disease drug product in vials or semi-finished syringes; 
Amyloid-targeted therapy for early Alzheimer's disease drug substance; 
Medicine delivery device, and parts thereof--including Cap Cartridge 
Holder, Dry Side Subassembly, Damping Cup, RNS Puller, Base Cap; 
Medicine delivery device needles; Glass vials; and Syringes (duty 
free).
    The request indicates that certain materials/components are subject 
to duties under section 232 of the Trade Expansion Act of 1962 or 
section 301 of the Trade Act of 1974, depending on the country of 
origin. The applicable section 232 and section 301 decisions require 
subject merchandise to be admitted to FTZs in privileged foreign status 
as described in 19 CFR 146.41.
    Public comment is invited from interested parties. Submissions 
shall be addressed to the Board's Executive Secretary and sent to: 
<a href="/cdn-cgi/l/email-protection#432537390337312227266d242c35"><span class="__cf_email__" data-cfemail="731507093307011217165d141c05">[email&#160;protected]</span></a>. The closing period for their receipt is November 4, 
2026.
    A copy of the notification will be available for public inspection 
in the ``Online FTZ Information System'' section of the Board's 
website.
    For further information, contact John Frye at <a href="/cdn-cgi/l/email-protection#2c66434442026a5e55496c585e4d4849024b435a"><span class="__cf_email__" data-cfemail="8dc7e2e5e3a3cbfff4e8cdf9ffece9e8a3eae2fb">[email&#160;protected]</span></a>.

    Dated: September 22, 2026.
Colin Agostisi,
Executive Secretary.
[FR Doc. 2026-19698 Filed 9-24-26; 8:45 am]
BILLING CODE 3510-DS-P


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Indexed from Federal Register on September 25, 2026.

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