Home / Import refusals / AEK-9028838-0/110003/1

FDA Import Refusal AEK-9028838-0/110003/1 — Sun Pharma Laboratories Ld

Sun Pharma Laboratories Ld — FEI 3016067500

The FDA refused shipment AEK-9028838-0/110003/1 from Sun Pharma Laboratories Ld (India) on December 5, 2025. The refused product falls under Drugs and Biologics — CARVEDILOL (ANTI-HYPERTENSIVE - PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 5, 2025
Country
India
Product Category
Drugs and Biologics
Product Code
62ODA22 CARVEDILOL (ANTI-HYPERTENSIVE - PART II)
Charges
75

Other import refusals

  • AEK-0454267-5/10002/1 (Sun May 31 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9426366-0/150003/1 (Fri Feb 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9170291-8/50003/1 (Fri Jan 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7900194-5/10003/1 (Thu Oct 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7635939-5/20002/1 (Mon Oct 27 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources