Appco Pharma LLC recalls Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
Recalled January 29, 2025 · FDA recall D-0208-2025 · Appco Pharma
Hazard
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet · FDA Class III
Units
1380 bottles
Sold at
Nationwide USA.
Description
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Product
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
Manufacturer(s)
Appco Pharma LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →