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Sun Pharma’s arm recalls some batches of Venlafaxine Hydrochloride tablets from US market

11 Jul 2014 Evaluate

Sun Pharmaceutical Industries’ subsidiary Caraco Pharmaceutical Laboratories has started recalling some batches of Venlafaxine Hydrochloride extended-release tablets from the US market.  According to a notification by the USFDA, the recall of 26,530 units of 30-count bottles and 14,597 units of 90-count bottles is voluntarily initiated by the company through a letter to the regulator last month under 'Class-II' classification. Venlafaxine Hydrochloride extended-release tablets are indicated for the treatment of major depressive disorder.

Sun Pharmaceutical Industries is an international, integrated, specialty pharmaceutical company. It manufactures and markets a large basket of pharmaceutical formulations as branded generics as well as generics in India, US and several other markets across the world.

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