Lupin Arm Recalls 5,720 Skin Treatment Cream Tubes In US

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Lupin's manufacturing site at Visakhapatnam. (Photo: Company website)

Drug maker Lupin is recalling 5,720 tubes of a cream used in the treatment of various skin conditions, such as dermatitis, eczema and psoriasis, from the US market due to a manufacturing issue, according to the U.S. Food and Drug Administration.

As per the latest Enforcement Report by the U.S. health regulator, Lupin Pharmaceuticals Inc, a U.S.-based arm of the Mumbai-based drug maker, is recalling Clobetasol propionate Cream, a steroid to reduce inflammation, redness and itchiness of the skin and prevent further irritation of the skin.

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The affected lot has been manufactured at the company's Pithampur plant in Madhya Pradesh and marketed in the U.S. market by Baltimore-based Lupin Pharmaceuticals Inc.

The U.S. FDA noted that the company is recalling the affected lot due to "Subpotent Drug: Low assay result observed during long-term stability testing".

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The company initiated the Class III nationwide (US) recall of the affected lot on January 23 this year.

As per the U.S. FDA, a class III recall is initiated in a "situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences".

The US generic drug market was estimated to be around $115.2 billion in 2019. It is the largest market for pharmaceutical products.

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