Drug recall D-0208-2025
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
Lots and codes
Lot #: 2402101UR, Exp 02/28/2027
Recall details
- Recalling firm
- Appco Pharma LLC, Piscataway, NJ
- Quantity
- 1380 bottles
- Distribution
- Nationwide USA.
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 16, 2025
Related products
- Venlafaxine – drug information
- NDC 43598-944 Venlafaxine · Venlafaxine Hydrochloride 225 mg/1 · Dr. Reddy's Laboratories Inc.
- NDC 43598-943 Venlafaxine · Venlafaxine Hydrochloride 150 mg/1 · Dr. Reddy's Laboratories Inc.