Recall
FDAHealthJanuary 16, 2025

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

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
January 16, 2025

Nationwide USA.

What's affected?

Product
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
UPC
0343598943909
Lot code
2402101UR

Additional details

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

What should I do?

Recommended action

Class III recall. Voluntary: Firm initiated Quantity affected: 1380 bottles.

View original FDA notice →

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