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FDA Import Refusal 112-4141252-0/1/1 — Wyeth Pharmaceuticals Llc

Wyeth Pharmaceuticals Llc — FEI 3004393730

The FDA refused shipment 112-4141252-0/1/1 from Wyeth Pharmaceuticals Llc (United States) on September 3, 2008. The refused product falls under Drugs and Biologics — VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal Details

Date
September 3, 2008
Country
United States
Product Category
Drugs and Biologics
Product Code
61NBP80 VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT)
Charges
75

Recent inspections

  • 1302588 (NAI Tue Apr 07 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1031032 (NAI Tue Aug 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 844357 (NAI Thu Aug 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 834523 (VAI Thu Jun 06 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 668809 (NAI Thu Jun 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • 1FX-3163017-0/10002/1 (Wed Apr 15 2026 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 799-0129510-6/11/8 (Tue Apr 09 2024 00:00:00 GMT+0000 (Coordinated Universal Time) — Human Foods)
  • 8JB-0093850-4/11/55 (Wed Mar 22 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 112-2441278-8/1/41 (Tue Sep 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • 112-7893560-1/2/1 (Mon Jul 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources