Home / Import refusals / AEK-7988892-9/30003/1

FDA Import Refusal AEK-7988892-9/30003/1 — Microlabs Limited

Microlabs Limited — FEI 3012264735

The FDA refused shipment AEK-7988892-9/30003/1 from Microlabs Limited (India) on December 9, 2025. The refused product falls under Drugs and Biologics — LEVETIRACETAM (ANTI-CONVULSANT). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 9, 2025
Country
India
Product Category
Drugs and Biologics
Product Code
61MCC42 LEVETIRACETAM (ANTI-CONVULSANT)
Charges
75

Other import refusals

  • AEK-9687524-8/50002/1 (Wed Sep 16 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0349073-6/170002/1 (Mon May 04 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7983679-5/30003/1 (Mon Jan 26 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-7983679-5/20003/1 (Mon Jan 26 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-0223139-5/21/1 (Thu Jan 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources