Recall D-0208-2025

US Class III Completed · initiated 2025-01-16

Recalling firm

Appco Pharma LLC, NJ

Product

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

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