Home / Import refusals / AEK-0461019-1/10002/1

FDA Import Refusal AEK-0461019-1/10002/1 — SUN PHARMA LABORATORIES LTD

SUN PHARMA LABORATORIES LTD — FEI 3042616197

The FDA refused shipment AEK-0461019-1/10002/1 from SUN PHARMA LABORATORIES LTD (India) on May 31, 2026. The refused product falls under Drugs and Biologics — LEVOCETIRIZINE DIHYDROCHLORIDE. Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
May 31, 2026
Country
India
Product Category
Drugs and Biologics
Product Code
61XCA51 LEVOCETIRIZINE DIHYDROCHLORIDE
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-0544441-8/10002/1 (Tue Jun 02 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