The U.S. Food and Drug Administration (FDA) has discontinued Mylan Pharmaceuticals' potassium chloride tablet, extended release, in 10 meq and 8 meq dosages. Mylan Pharmaceuticals is a subsidiary of Viatris Inc.
The specific reasons for the FDA's discontinuation of this product were not detailed in the available information. This action by the regulatory body impacts the availability of the product in the market.
The discontinuation of an actively distributed product can lead to a loss of revenue for Viatris. This event underscores the continuous regulatory oversight in the pharmaceutical industry and the potential for product portfolio adjustments based on FDA decisions.
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