Appco Pharma LLC: Drug Recall
Recall #D-0208-2025 · 01/16/2025
Class III: Low Risk
Recall Details
- Recall Number
- D-0208-2025
- Classification
- Class III
- Product Type
- Drug
- Recalling Firm
- Appco Pharma LLC
- Status
- Completed
- Date Initiated
- 01/16/2025
- Location
- Piscataway, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1380 bottles
Reason for Recall
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Product Description
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
Distribution Pattern
Nationwide USA.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.