Lucid Pharmaceuticals recalled more than 69,000 bottles of its extended-release antidepressant drug cenlafaxine hydrochloride over quality concerns.
Here are three things to know.
- Lucid launched the nationwide voluntary recall June 1 after receiving complaints from pharmacists about melted drug capsules.
- The recall applies to 30-count and 90-count bottles of the antidepressant.
- The Food and Drug Administration announced the recall last week, labeling it as a Class II event, meaning the quality issue poses an intermediate threat of illness or death.
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