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FDA Import Refusal AEK-0544441-8/10002/1 — SUN PHARMA LABORATORIES LTD

SUN PHARMA LABORATORIES LTD — FEI 3017005182

The FDA refused shipment AEK-0544441-8/10002/1 from SUN PHARMA LABORATORIES 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

  • 1FX-7508637-0/10002/1 (Thu Jul 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 1FX-0103353-9/30002/1 (Fri Jun 26 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0461019-1/10002/1 (Sun May 31 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0349073-6/200002/1 (Mon May 04 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9487413-6/10003/1 (Mon Mar 09 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources