Class III

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

Appco Pharma LLC · January 16, 2025

Reason for Recall

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

Distribution

Nationwide USA.

States Affected

NATIONWIDE

Quantity Affected

1380 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0208-2025

Status: completed

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.