Imipramine Pamoate Capsules 125 mg, 30-count bottle, Rx only, Manufactured for Lupin Pharmaceuticals, Inc. Baltimore, Maryland…
Reason Out of specification result observed in a dissolution test at the 9-month long term stability time point.
5 FDA recalls mention Imipramine. The most recent are listed below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Imipramine.
Reason Out of specification result observed in a dissolution test at the 9-month long term stability time point.
Reason Chemical Contamination; benzophenone leached from the product label varnish
Reason Chemical Contamination; benzophenone leached from the product label varnish
Reason Chemical Contamination; benzophenone leached from the product label varnish
Reason Labeling: Label Mixup: IMIPRAMINE HCL, Tablet, 25 mg may have potentially been mislabeled as the following drug: FENOFIBRATE, Tablet, 54 mg, NDC…
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