
Lupin Launches Bosentan Tablets for Oral Suspension in the US with 180-Day Exclusivity
Global pharma major Lupin Limited has announced the launch of Bosentan Tablets for Oral Suspension, 32 mg in the United States. This launch follows the approval received by Lupin’s alliance partner, NATCO Pharma Limited for its Abbreviated New Drug Application from the U.S. Food and Drug Administration. NATCO holds the exclusive first-to-file status for this product and will have 180-day generic drug exclusivity. Bosentan Tablets for Oral Suspension are bioequivalent to Tracleer® Tablets for Oral Suspension of Actelion Pharmaceuticals US, Inc. They are indicated for the treatment of pulmonary arterial hypertension (PAH) in pediatric patients aged 3 years and older with idiopathic or congenital PAH to improve pulmonary vascular resistance. Bosentan Tablets (RLD Tracleer®) had estimated annual sales of USD 10 million in the U.S. (IQVIA MAT June 2025).
Key Highlights
- Lupin launches Bosentan Tablets for Oral Suspension in the US
- Follows approval from U.S. FDA for NATCO's Abbreviated New Drug Application
- Exclusive first-to-file status for NATCO with 180-day generic drug exclusivity
- Indicated for treatment of pulmonary arterial hypertension in pediatric patients
- Estimated annual sales of USD 10 million in the U.S.