Home / Import refusals / AEK-0516421-3/41/1

FDA Import Refusal AEK-0516421-3/41/1 — Hetero Labs Ltd

Hetero Labs Ltd — FEI 3007785633

The FDA refused shipment AEK-0516421-3/41/1 from Hetero Labs Ltd (India) on March 12, 2022. The refused product falls under Drugs and Biologics — IVERMECTIN (ANTI-PROTOZOAL, A-LEISHMANIAL, ANTI-MALARIAL). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 12, 2022
Country
India
Product Category
Drugs and Biologics
Product Code
62LDY47 IVERMECTIN (ANTI-PROTOZOAL, A-LEISHMANIAL, ANTI-MALARIAL)
Charges
75

Recent inspections

  • 1120998 (NAI Fri Feb 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-9410963-2/40002/1 (Mon Mar 16 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-9426366-0/70003/1 (Fri Feb 06 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-9272027-0/10003/1 (Fri Nov 21 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • SCS-8566337-0/10002/1 (Wed Oct 22 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7261494-2/23/1 (Wed Jul 02 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources