Home / Import refusals / AEK-0544441-8/20002/1

FDA Import Refusal AEK-0544441-8/20002/1 — GLENMARK PHARMACEUTICALS LTD

GLENMARK PHARMACEUTICALS LTD — FEI 3019089903

The FDA refused shipment AEK-0544441-8/20002/1 from GLENMARK PHARMACEUTICALS LTD (India) on June 2, 2026. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
June 2, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
62ODY09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

Other import refusals

  • AEK-7293172-6/22/1 (Thu Aug 14 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-5820617-0/11/3 (Wed Feb 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-5877716-8/61/1 (Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-2868330-0/11/7 (Mon Sep 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-4893039-8/31/1 (Thu Mar 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

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