4 FDA recalls mention Lovastatin. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Lovastatin.
Reason CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Reason CGMP Deviations: Finished product made with lovastatin drug substance that was out of specification for individual impurity results.
Reason Failed Dissolution Specifications: Low out of specification results for dissolution during annual stability testing.
Reason Labeling: Label Mixup: LOVASTATIN, Tablet, 20 mg may have potentially been mislabeled as one of the following drugs: ASPIRIN EC DR, Tablet, 81 mg…
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