Valeant Pharmaceuticals North America LLC Recall: Fenoglide (fenofibrate) tablets, 120 mg
Valeant Pharmaceuticals North America LLC Recall: Fenoglide (fenofibrate) tablets, 120 mg is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Valeant Pharmaceuticals North America LLC; Product: Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus
| Recalling firm | Valeant Pharmaceuticals North America LLC |
|---|---|
| Product | Fenoglide (fenofibrate) tablets, 120 mg Tablets, 90 Ct Bottle, Rx Only. Distributed by: Santarus, Inc. San Diego, CA 92130. NDC: 68012-495-90. |
| Reason for recall | Failed Dissolution Specifications: Failed 24 month dissolution testing. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | U.S. Nationwide |
| Recall initiated | 20150904 |
| Recall number | D-0163-2016 |
| Category | drug |
| State | NJ |
| Country | United States |
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