FDAFDA · Food and drugs·Recall number D-0208-2025
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
Published January 29, 2025 · Recall initiated: January 16, 2025
Status when published: Completed — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VENLAFAXINE
- Manufacturer
- Appco Pharma LLC
- Distributor
- Nationwide USA.
- UPC
- 0343598943909
- Lot
- Lot #: 2402101UR, Exp 02/28/2027
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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