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.
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