
Biocon Limited announced that its wholly owned subsidiary Biocon Pharma Limited has received approval from the U.S. Food and Drug Administration (U.S. FDA) for its Liraglutide Injection (gVictoza®). The approval relates to the 18 mg/3 mL (6 mg/mL) formulation available in single-patient-use prefilled pens.
Liraglutide is prescribed for the treatment of Type 2 Diabetes Mellitus in adults, adolescents and children aged 10 years and above whose blood sugar levels are not adequately controlled. The therapy is typically used alongside diet and exercise as part of a broader diabetes management programme.
The approval comes shortly after the company secured approval for another Liraglutide-based product (gSaxenda®) on February 24, 2026. The latest clearance strengthens Biocon’s range of complex, vertically integrated pharmaceutical products, particularly in the metabolic and diabetes therapy segment.
Biocon Limited is a global biopharmaceutical company headquartered in Bengaluru, India. The company focuses on the development and manufacturing of biosimilars, generic formulations and complex biologics across therapeutic areas such as diabetes, oncology and immunology. Through its subsidiaries and global partnerships, Biocon supplies medicines to multiple international markets.
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As of 13 March 2026, at 11:18 AM, Biocon Limited share price is trading at ₹384.35 per share, reflecting a decline of 2.0% from the previous closing price. Over the past month, the stock has gained by 1.69%.
The approval of Liraglutide Injection expands Biocon’s diabetes treatment portfolio and strengthens its presence in global pharmaceutical markets. It also reflects the company’s continued focus on developing therapies in the metabolic and diabetes treatment segment.
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Published on: Mar 13, 2026, 12:45 PM IST

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