Lupin gets US FDA nod for Dronedarone Tablets, USP
They are indicated to reduce the risk of hospitalisation for atrial fibrillation (AF) in patients in sinus rhythm with a history of paroxysmal or persistent AF
Lupin has received approval from the United States Food and Drug Administration (US FDA) for its Abbreviated New Drug Application for Dronedarone Tablets USP, 400 mg, to market a generic equivalent of Multaq Tablets, 400 mg of Sanofi-Aventis US. The product will be manufactured at Lupin’s Goa facility in India.
Dronedarone Tablets USP, 400 mg, are indicated to reduce the risk of hospitalisation for atrial fibrillation (AF) in patients in sinus rhythm with a history of paroxysmal or persistent AF.
Dronedarone Tablets (RLD Multaq) had estimated annual sales of $510 million in the US (IQVIA MAT December 2023).