Home / Import refusals / AEK-7732651-8/10002/1

FDA Import Refusal AEK-7732651-8/10002/1 — Viatris Pharmaceuticals LLC

Viatris Pharmaceuticals LLC — FEI 2623619

The FDA refused shipment AEK-7732651-8/10002/1 from Viatris Pharmaceuticals LLC (United States) on November 14, 2025. The refused product falls under Drugs and Biologics — VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT). Cited charges: 118,75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
November 14, 2025
Country
United States
Product Category
Drugs and Biologics
Product Code
61NCY80 VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT)
Charges
118,75

Recent inspections

  • 1290796 (VAI Mon May 18 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1162864 (VAI Thu Feb 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1038692 (VAI Fri Jan 26 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 990477 (VAI Tue Jul 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933988 (VAI Fri Jun 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • AEK-5902776-1/41/1 (Mon Dec 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-4692799-0/11/1 (Wed Feb 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-3057736-3/41/1 (Fri May 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-2594296-0/41/1 (Fri Jan 27 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-2684768-9/11/1 (Fri Jan 20 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources