Lupin has recalled a single lot of Pravastatin Sodium USP tablets from the US market. Pravastatin Sodium is indicated for reducing levels of bad cholesterol and triglycerides in the blood.
According to the US Food and Drug Administration (USFDA), the company is voluntarily recalling the product due to a pharmacy complaint where one Duloxetine delayed-release capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle. The ongoing Class II recall was initiated on November 17.
Lupin is an innovation led transnational pharmaceutical company developing and delivering a wide range of branded & generic formulations, biotechnology products and APIs globally.