Notice2026-09715

Glycine From India: Preliminary Results and Rescission, in Part, of Antidumping Duty Administrative Review; 2024-2025

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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
May 14, 2026

Issuing agencies

Commerce DepartmentInternational Trade Administration

Abstract

The U.S. Department of Commerce (Commerce) preliminarily determines that producers and/or exporters subject to this administrative review made sales of subject merchandise at less than normal value (NV) during the period of review (POR), June 1, 2024, through May 31, 2025. In addition, we are rescinding the review with respect to 27 companies. Interested parties are invited to comment on these preliminary results.

Full Text

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<title>Federal Register, Volume 91 Issue 93 (Thursday, May 14, 2026)</title>
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[Federal Register Volume 91, Number 93 (Thursday, May 14, 2026)]
[Notices]
[Pages 27262-27264]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-09715]


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DEPARTMENT OF COMMERCE

International Trade Administration

[A-533-883]


Glycine From India: Preliminary Results and Rescission, in Part, 
of Antidumping Duty Administrative Review; 2024-2025

AGENCY: Enforcement and Compliance, International Trade Administration, 
Department of Commerce.

SUMMARY: The U.S. Department of Commerce (Commerce) preliminarily 
determines that producers and/or exporters subject to this 
administrative review made sales of subject merchandise at less than 
normal value (NV) during the period of review (POR), June 1, 2024, 
through May 31, 2025. In addition, we are rescinding the review with 
respect to 27 companies. Interested parties are invited to comment on 
these preliminary results.

DATES: Applicable May 14, 2026.

FOR FURTHER INFORMATION CONTACT: Tyler Weinhold, AD/CVD Operations, 
Office VI, Enforcement and Compliance, International Trade 
Administration, U.S. Department of Commerce, 1401 Constitution Avenue 
NW, Washington, DC 20230; telephone: (202) 482-1121.

SUPPLEMENTARY INFORMATION:

Background

    On July 25, 2025, based on timely requests for review, in 
accordance with 19 CFR 351.221(c)(1)(i), we initiated an administrative 
review the antidumping duty order on glycine from India.\1\ On 
September 10, 2026, Commerce selected Avid Organics Private Limited 
(Avid) and Mulji Mehta Enterprises (Mulji Mehta) as the mandatory 
respondents in this review.\2\ On October 23, 2025, Avid timely 
withdrew its request for review of itself; \3\ and DPG timely withdrew 
its administrative review requests for certain companies identified in 
the Initiation Notice, including Avid.\4\ Further, on December 5, 2025, 
Paras Intermediates Private Limited timely withdrew its review request 
for itself.\5\ On December 9, 2025, Commerce selected Medilane 
Healthcare Private Limited (Medilane), the only other company subject 
to this review in addition to Mulji Mehta, as an additional mandatory 
respondent.\6\
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    \1\ See Initiation of Antidumping and Countervailing Duty 
Administrative Reviews, 90 FR 35268 (July 25, 2025) (Initiation 
Notice); see also Glycine from India and Japan: Amended Final 
Affirmative Antidumping Duty Determination and Antidumping duty 
Orders, 84 FR 29170 (June 21, 2019) (Order).
    \2\ See Memorandum, ``Respondent Selection,'' dated September 
10, 2025.
    \3\ See Avid's Letter, ``Withdrawal of Review Request of Anti-
Dumping Duty Administrative Review for review period 2024-2025,'' 
dated October 23, 2025.
    \4\ See DPG's Letter, ``Partial Withdrawal of Request for 
Administrative Review,'' dated October 23, 2025; see also DPG's 
Letter, ``Corrected Partial Withdrawal of Request for Administrative 
Review,'' dated December 8, 2025.
    \5\ See Paras' Letter, ``Withdrawal of Review Request for Anti-
Dumping Duty Administrative Review,'' dated December 5, 2025.
    \6\ See Memorandum, ``Selection of Medilane Healthcare Private 
Limited as a Mandatory Respondent,'' dated December 9, 2025.
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    Due to the lapse in appropriations and Federal Government shutdown, 
on November 14, 2025, Commerce tolled all deadlines in administrative 
proceedings by 47 days.\7\ Additionally, due to a backlog of documents 
that were electronically filed via Enforcement and Compliance's 
Antidumping and Countervailing Duty Centralized Electronic Service 
System (ACCESS) during the Federal Government shutdown, on November 24, 
2025, Commerce tolled all deadlines in administrative proceedings by an 
additional 21 days.\8\ On December 22, 2025, Commerce extended the time 
limit for these preliminary results in accordance with section 
751(a)(3)(A).\9\ Accordingly, the deadline for these preliminary 
results is now May 11, 2026.
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    \7\ See Memorandum, ``Deadlines Affected by the Shutdown of the 
Federal Government,'' dated November 14, 2025.
    \8\ See Memorandum, ``Tolling of all Case Deadlines,'' dated 
November 24, 2025.
    \9\ See Memorandum, ``Extension of Deadline for Preliminary 
Results of Antidumping Duty Administrative Review,'' dated December 
22, 2025.
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    For a complete description of the events that followed the 
initiation of this review, see the Preliminary Decision Memorandum.\10\ 
A list of the topics discussed in the Preliminary Decision Memorandum 
is attached as Appendix I to this notice. The Preliminary Decision 
Memorandum is a public document and is on file electronically via 
Enforcement and Compliance's Antidumping and Countervailing Duty 
Centralized Electronic Service System (ACCESS). ACCESS is available to 
registered users at <a href="https://access.trade.gov">https://access.trade.gov</a>. In addition, a complete 
version of the Preliminary Decision Memorandum can be accessed directly 
at <a href="https://access.trade.gov/frnotices">https://access.trade.gov/frnotices</a>.
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    \10\ See Memorandum, ``Decision Memorandum for the Preliminary 
Results of the Administrative Review of the Antidumping Duty Order 
on Glycine from India; 2024-2025,'' dated concurrently with, and 
hereby adopted by, this notice (Preliminary Decision Memorandum).
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Scope of the Order

    The merchandise subject to the Order is glycine from India. For a 
complete description of the scope of the Order, see the Preliminary 
Decision Memorandum.

Rescission of Administrative Review, in Part

    Pursuant to 19 CFR 351.213(d)(1), Commerce will rescind an 
administrative review, in whole or in part, if a party who requested a 
review withdraws its request within 90 days of the date of publication 
of notice of initiation. As noted above, Commerce received timely-filed 
withdrawal requests with respect to the companies listed in Appendix 
II, and no other parties requested an administrative review of these 
companies. Therefore, we are rescinding this administrative review with 
respect to these companies, pursuant to 19 CFR 351.213(d)(1).

[[Page 27263]]

Methodology

    Commerce is conducting this review in accordance with section 
751(a) of the Tariff Act of 1930, as amended (the Act). In addition, 
Commerce has relied entirely on facts available with adverse inferences 
under sections 776(a) and (b) of the Act for Medilane Healthcare 
Private Limited and Mulji Mehta. For a full description of the 
methodology underlying our conclusions, see the Preliminary Decision 
Memorandum.

Preliminary Results of Review

    As a result of this review, we preliminarily determine the 
following estimated weighted-average dumping margins exist for the 
period June 1, 2024, through May 31, 2025:

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                                                       Weighted- average
                  Producer/exporter                      dumping margin
                                                           (percent)
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Medilane Healthcare Private Limited..................              57.17
Mulji Mehta Enterprises..............................              57.17
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Disclosure

    Normally, Commerce discloses to interested parties the calculations 
performed in preliminary results within five days of any public 
announcement or, if there is no public announcement, within five days 
of the date of publication of the notice of preliminary results in the 
Federal Register, in accordance with 19 CFR 351.224(b). However, 
because Commerce preliminarily applied adverse facts available with 
adverse inferences to the individually examined companies, in 
accordance with section 776 of the Act, there are no calculations to 
disclose.

Public Comment

    Case briefs or other written comments may be submitted to the 
Assistant Secretary for Enforcement and Compliance. Pursuant to 19 CFR 
351.309(c)(1)(ii), we have modified the deadline for interested parties 
to submit case briefs to Commerce to no later than 21 days after the 
date of the publication of this notice.\11\ Rebuttal briefs, limited to 
issues raised in the case briefs, may be filed not later than five days 
after the date for filing case briefs.\12\ Interested parties who 
submit case briefs or rebuttal briefs in this proceeding must submit: 
(1) a table of contents listing each issue; and (2) a table of 
authorities.\13\
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    \11\ See 19 CFR 351.309.
    \12\ See 19 CFR 351.309(d); see also Administrative Protective 
Order, Service, and Other Procedures in Antidumping and 
Countervailing Duty Proceedings, 88 FR 67069, 67077 (September 29, 
2023) (APO and Service Procedures).
    \13\ See 19 CFR 351.309(c)(2) and (d)(2).
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    As provided under 19 CFR 351.309(c)(2)(iii) and (d)(2)(iii), we 
request that interested parties provide at the beginning of their 
briefs a public executive summary for each issue raised in their 
briefs.\14\ Further, we request that interested parties limit their 
public executive summary of each issue to no more than 450 words, not 
including citations. We intend to use the public executive summaries as 
the basis of the comment summaries included in the issues and decision 
memorandum that will accompany the final results in this administrative 
review. We request that interested parties include footnotes for 
relevant citations in the public executive summary of each issue. Note 
that Commerce has amended certain of its requirements pertaining to the 
service of documents in 19 CFR 351.303(f).\15\
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    \14\ We use the term ``issue'' here to describe an argument that 
Commerce would normally address in a comment of the Issues and 
Decision Memorandum.
    \15\ See APO and Service Procedures.
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    Pursuant to 19 CFR 351.310(c), interested parties who wish to 
request a hearing must submit a written request to the Assistant 
Secretary for Enforcement and Compliance, filed electronically via 
ACCESS by 5:00 p.m. Eastern Time within 30 days after the date of 
publication of this notice. Requests should contain: (1) the party's 
name, address, and telephone number; (2) the number of participants; 
and (3) a list of issues to be discussed. Oral presentations at the 
hearing will be limited to issues raised in the briefs. If a request 
for a hearing is made, Commerce will inform parties of the scheduled 
date for the hearing.\16\
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    \16\ See 19 CFR 351.310(d).
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    All submissions, including case and rebuttal briefs, as well as 
hearing requests, should be filed via ACCESS.\17\ An electronically 
filed document must be received successfully in its entirety by ACCESS 
by 5:00 p.m. Eastern Time on the established deadline.
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    \17\ See 19 CFR 351.303.
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Assessment Rates

    Pursuant to section 751(a)(2)(A) of the Act and 19 CFR 
351.212(b)(1), Commerce shall determine, and U.S. Customs and Border 
Protection (CBP) shall assess, antidumping duties on all appropriate 
entries of subject merchandise in accordance with the final results of 
this review.
    If the mandatory respondent's weighted-average dumping margin is 
not zero or de minimis (i.e., less than 0.50 percent) in the final 
results of this review, Commerce intends to calculate importer-specific 
assessment rates on the basis of the ratio of the total amount of 
dumping calculated for each importer's examined sales to the total 
entered value of those sales. Where we do not have entered values for 
all U.S. sales to a particular importer, we will calculate an importer-
specific, per-unit assessment rate on the basis of the ratio of the 
total amount of dumping calculated for the importer's examined sales to 
the total quantity of those sales.\18\ To determine whether an 
importer-specific, per-unit assessment rate is de minimis, in 
accordance with 19 CFR 351.106(c)(2), we also will calculate an 
importer-specific ad valorem ratio based on estimated entered values. 
If the mandatory respondents' weighted-average dumping margin is zero 
or de minimis in the final results of review, or if an importer-
specific assessment rate is zero or de minimis, Commerce will instruct 
CBP to liquidate appropriate entries without regard to antidumping 
duties.\19\
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    \18\ See 19 CFR 351.212(b)(1).
    \19\ Id.; see also 77 FR at 8102-03; see also 19 CFR 
351.106(c)(2).
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    In accordance with Commerce's ``automatic assessment'' practice, 
for entries of subject merchandise during the POR produced by the 
mandatory respondents for which they did not know that the merchandise 
was destined for the United States, we intend to instruct CBP to 
liquidate those entries at the all-others rate calculated in the less-
than-fair-value (LTFV) investigation if there is no rate for the 
intermediate companies involved in the transaction.\20\
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    \20\ For a full discussion of this practice, see Antidumping and 
Countervailing Duty Proceedings: Assessment of Antidumping Duties, 
68 FR 23954 (May 6, 2003).
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    For the companies listed in Appendix II for which the review is 
being rescinded, Commerce will instruct CBP to assess antidumping 
duties on all appropriate entries. Antidumping duties shall be assessed 
at rates equal to the cash deposit rate for estimated antidumping 
duties required at the time of entry, or withdrawal from warehouse, for 
consumption, in accordance with 19 CFR 351.212(c)(1)(i). Commerce 
intends to issue rescission instructions to CBP no earlier than 35 days 
after the date of publication of this notice in the Federal Register.
    Commerce intends to issue assessment instructions to CBP regarding 
Medilane and Mulji Mehta no earlier than 35 days after the date of 
publication of the final results of this review in the Federal 
Register. If a

[[Page 27264]]

timely summons is filed at the U.S. Court of International Trade, the 
assessment instructions will direct CBP not to liquidate relevant 
entries until the time for parties to file a request for a statutory 
injunction has expired (i.e., within 90 days of publication).

Cash Deposit Requirements

    The following cash deposit requirements will be effective upon 
publication in the Federal Register of the final results of this 
administrative review for all shipments of the subject merchandise 
entered, or withdrawn from warehouse, for consumption on or after the 
date of publication, as provided by section 751(a)(2)(C) of the Act: 
(1) the cash deposit rate for companies listed above will be that 
established in the final results of this review, except if the rate is 
less than 0.50 percent and, therefore, de minimis within the meaning of 
19 CFR 351.106(c)(1), in which case the cash deposit rate will be zero; 
(2) for previously investigated or reviewed companies not covered by 
this review, the cash deposit rate will continue to be the company-
specific cash deposit rate published for the most recently completed 
segment of this proceeding in which the company participated; (3) if 
the exporter is not a firm covered in this review, a prior review, or 
the LTFV investigation but the manufacturer is, then the cash deposit 
rate will be the rate established in the most recently completed 
segment of the proceeding for the producer of the merchandise; and (4) 
the cash deposit rate for all other manufacturers or exporters will 
continue to be 7.23 percent, the all-others rate established in the 
LTFV investigation.\21\ These cash deposit requirements, when imposed, 
shall remain in effect until further notice.
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    \21\ See Order.
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Notification to Importers

    This notice also serves as a preliminary reminder to importers of 
their responsibility under 19 CFR 351.402(f)(2) to file a certificate 
regarding the reimbursement of antidumping and/or countervailing duties 
prior to liquidation of the relevant entries during this review period. 
Failure to comply with this requirement could result in Commerce's 
presumption that reimbursement of antidumping and/or countervailing 
duties occurred and the subsequent assessment of double antidumping 
duties, and/or an increase in the amount of antidumping duties by the 
amount of the countervailing duties.

Notification to Interested Parties

    We are issuing and publishing these preliminary results of review 
in accordance with sections 751(a)(1) and 777(i)(1) of the Act, and 19 
CFR 351.221(b)(4).

    Dated: May 11, 2026.
Christopher Abbott,
Deputy Assistant Secretary for Policy Assistant Secretary, performing 
the non-exclusive functions and duties of the Assistant Secretary for 
Enforcement and Compliance.

Appendix I

List of Topics Discussed in the Preliminary Decision Memorandum

I. Summary
II. Background
III. Scope of the Order
IV. Application of Facts Available and Use of Adverse Inferences
V. Recommendation

Appendix II

Companies for Which the Review Has Been Rescinded

1. Aditya Chemicals
2. Adwith Nutrichem Private Limited
3. Avid Organics Private Limited (Avid)
4. Bajaj Healthcare Limited
5. Elementis Specialties India Private Limited
6. Euroasias Organics Private Limited
7. Euroasia Trans Continental
8. Galaxy Surfactants Limited
9. Glisten Biotech
10. Grauer & Weil (India) Limited
11. Gujarat Ambuja Export Limited
12. Gulbrandsen Technologies (India) Private Limited
13. Indiana Chem Port
14. Kronox Lab Sciences Private Limited
15. Mass Dye Chem. Private Limited
16. Meteoric Biopharmaceuticals Private Limited
17. Mulji Mehta Pharma
18. Mumbai Merchant
19. Nature Bio
20. Paras Intermediates Private Limited
21. Priya Chemicals
22. Promois International Limited
23. Shari Pharmachem Private Limited
24. Strava Healthcare Private Limited
25. Tarkesh Trading Company
26. Valaji Pharma Chem
27. Venus International Exports Private Limited

[FR Doc. 2026-09715 Filed 5-13-26; 8:45 am]
BILLING CODE 3510-DS-P


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Indexed from Federal Register on May 14, 2026.

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