WhichRecall
Class IIIReported 2025-01-29

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

Recalled by Appco Pharma LLC

Reason for Recall

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

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Recall Number
D-0208-2025
Classification
Class III
Status
Completed
Category
drug
Initiated
2025-01-16
Reported
2025-01-29
Distribution
Nationwide USA.
Code Info
Lot #: 2402101UR, Exp 02/28/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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