Appco Pharma LLC recalls Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
- Recall date
- January 16, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0208-2025
- FDA classification
- Class III
- Brand / firm
- Appco Pharma LLC
- Sold / distributed
- Nationwide USA.
Why it was recalled
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598-943-90.
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