Home / Recalls / Appco Pharma LLC / D-0208-2025

D-0208-2025 Class III

Recalled by Appco Pharma LLC — Piscataway, NJ

Recall Details

Product Type: Drugs
Report Date: January 29, 2025
Initiation Date: January 16, 2025
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 1380 bottles

Product Description

Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.

Reason for Recall

Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet

Distribution Pattern

Nationwide USA.

Code Information

Lot #: 2402101UR, Exp 02/28/2027