Home / Import refusals / AEK-7619218-3/21/1

FDA Import Refusal AEK-7619218-3/21/1 — Lupin Limited

Lupin Limited — FEI 3004529241

The FDA refused shipment AEK-7619218-3/21/1 from Lupin Limited (India) on July 27, 2020. 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
July 27, 2020
Country
India
Product Category
Drugs and Biologics
Product Code
62ODY09 TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
Charges
75

Recent inspections

  • 932466 (NAI Fri Jun 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-5916344-2/11/1 (Fri Dec 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-4906989-9/41/1 (Fri Mar 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-7029084-7/11/7 (Tue Oct 03 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-3661110-9/31/1 (Mon Jul 31 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-7725460-5/31/1 (Fri Mar 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources