Sun Pharmaceutical Industries Ltd
31 Jan 2026 12:00 AM
Board of Sun Pharmaceuticals Industries recommends interim dividend,
Sun Pharmaceuticals Industries announced that the Board of Directors of the Company at its meeting held on 31 January 2026, inter alia, have recommended the interim dividend of Rs 11 per equity Share (i.e. 1100%) , subject to the approval of the shareholders.Powered by Capital Market - Live News
Sun Pharmaceutical Industries Ltd
31 Jan 2026 12:00 AM
Sun Pharmaceutical Industries consolidated net profit rises 16.03% in the December 2025 quarter,
Net profit of Sun Pharmaceutical Industries rose 16.03% to Rs 3368.81 crore in the quarter ended December 2025 as against Rs 2903.38 crore during the previous quarter ended December 2024. Sales rose 15.12% to Rs 15469.07 crore in the quarter ended December 2025 as against Rs 13436.94 crore during the previous quarter ended December 2024. ParticularsQuarter EndedDec. 2025Dec. 2024% Var. Sales15469.0713436.94 15 OPM %31.9929.84 - PBDT5448.974423.13 23 PBT4716.643792.57 24 NP3368.812903.38 16 Powered by Capital Market - Live News
Sun Pharmaceutical Industries Ltd
23 Jan 2026 12:00 AM
Sun Pharma receives DCGI approval for generic version of semaglutide injection,
Sun Pharmaceutical Industries announced that it has received approval from the Drugs Controller General of India (DCGI) to manufacture and market a generic version of semaglutide injection. Semaglutide, a glucagon-like peptide-1 (GLP-1) receptor agonist, is indicated for chronic weight management in adults as an adjunct to a reduced calorie diet and increased physical activity. Sun Pharma will launch generic semaglutide injection under the brand name, Noveltreat, after the expiry of semaglutide patent in India. The product has received approval from the DCGI following a review of a Phase III clinical trial conducted in India. Noveltreat will be available in five dose strengths - 0.25 mg/0.5 mL, 0.5 mg/0.5 mL, 1 mg/0.5 mL, 1.7 mg/0.75 mL, and 2.4 mg/0.75 mL, with a maintenance dose of 2.4 mg once weekly. The product is administered via an easy-to-use prefilled pen, designed to support convenient and accurate dosing. �Obesity and diabetes have emerged as two of the most pressing health challenges confronting India and GLP-1 based therapies can play a meaningful role in addressing this growing burden. Noveltreat meets global quality standards and is supported by robust Indian clinical evidence on efficacy and safety for weight management. As India`s largest pharmaceutical company with leadership in cardiometabolic therapies, we are committed to improving access to generic semaglutide across the country after the patent expiry�, said Kirti Ganorkar, Managing Director, Sun Pharma.�GLP-1 receptor agonists like semaglutide are an important scientific advancement for overall metabolic health, not just weight. These treatments should be combined with appropriate lifestyle measures such as diet and physical activity. They should be taken under close medical supervision. We are seeing growing patient interest in this therapy, and improved accessibility will help address unmet needs�, said Dr. Unnikrishnan A G, Chief Endocrinologist and CEO, Chellaram Diabetes Institute. In December 2025, Sun Pharma received DCGI approval for manufacturing and marketing semaglutide injection for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise. It will be launched under the brand name Sematrinity, after the expiry of semaglutide patent in India.Powered by Capital Market - Live News
Sun Pharmaceutical Industries Ltd
21 Jan 2026 12:00 AM
Sun Pharmaceuticals Industries to convene board meeting,
Sun Pharmaceuticals Industries will hold a meeting of the Board of Directors of the Company on 31 January 2026.Powered by Capital Market - Live News
Sun Pharmaceutical Industries Ltd
18 Dec 2025 12:00 AM
USFDA classifies Sun Pharma`s Baska facility inspection as Official Action Indicated,
Sun Pharmaceutical Industries announced that the US FDA conducted an inspection at the Company`s Baska facility from 8 September 2025 to 19 September 2025. The US FDA has subsequently determined that the inspection classification status of this facility is Official Action Indicated (OAI). Powered by Capital Market - Live News
Subscribe for our
newsletter
newsletter
HSL Mobile App