DGTR Initiates Anti-Dumping Probe on TB Drug Ethambutol Hydrochloride from China and Thailand Following Complaint by Lupin Ltd, Supported by Cadila Pharma and Themis Medicare

·      Normal Value Constructed for both China and Thailand

[DGTR Initiation Notification Case No. AD (OI) – 22/2025 dated 23.09.2025]

Subject of Investigation

·         Product: Ethambutol Hydrochloride, a bacteriostatic drug used in treating pulmonary tuberculosis.

·         Countries Involved: People's Republic of China and the Kingdom of Thailand.

·         Purpose: To investigate alleged dumping of Ethambutol Hydrochloride into India and its impact on domestic industry.

Key Points

A. Product Details

·         Ethambutol Hydrochloride is derived from Ethambutol and used in tablet form due to better stability and solubility.

·         Classified under HS Code 29051490, though classification is indicative.

B. Like Article

·         The imported product is considered identical to the domestically produced version by Lupin Ltd.

C. Domestic Industry

·         Applicant: Lupin Limited.

·         Other producers: Cadila Pharmaceuticals (also an importer) and Themis Medicare (ceased production).

·         Lupin is deemed to represent 100% of eligible domestic production.

D. Period of Investigation

·         POI: April 1, 2024 – March 31, 2025.

·         Injury analysis includes data from 2021–2024.

E. Dumping Margin

·         China: Normal value constructed using Indian cost estimates due to lack of market economy evidence.

·         Thailand: Normal value also constructed using Indian cost estimates.

·         Export prices derived from DG Systems import data.

·         Preliminary findings suggest significant dumping margins above de minimis levels.

F. Injury Allegation

·         Imports are undercutting domestic prices, suppressing price increases, and causing financial harm to the domestic industry.

G. Initiation of Investigation

·         Based on prima facie evidence, DGTR initiates an anti-dumping investigation under Section 9A of the Customs Tariff Act.

H. Procedure & Submissions

·         Interested parties must submit relevant information within 30 days.

·         Confidential submissions must be accompanied by non-confidential versions and justification for confidentiality.

I. Non-Cooperation Clause

·         Parties failing to cooperate may be deemed non-cooperative, and findings may be based on available facts.