Home / Import refusals / AEK-4893039-8/31/1

FDA Import Refusal AEK-4893039-8/31/1 — GLENMARK PHARMACEUTICALS LTD

GLENMARK PHARMACEUTICALS LTD — FEI 3014779728

The FDA refused shipment AEK-4893039-8/31/1 from GLENMARK PHARMACEUTICALS LTD (India) on March 21, 2024. The refused product falls under Drugs and Biologics — MINOXIDIL (ANTI-HYPERTENSIVE). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 21, 2024
Country
India
Product Category
Drugs and Biologics
Product Code
62CDL41 MINOXIDIL (ANTI-HYPERTENSIVE)
Charges
75

Other import refusals

  • AEK-0544441-8/20002/1 (Tue Jun 02 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 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)

FDA data resources