Cipla strengthens US portfolio with the launch of generic Saxenda® (Liraglutide Injection) for weight management therapy
Rhea-AI Summary
Cipla (OTC: CPLFY) announced the U.S. launch of generic Liraglutide Injection (18 mg/3 mL), the equivalent of Saxenda®, after partner Orbicular secured USFDA ANDA approval. Cipla will lead U.S. marketing and distribution and says the product will be available immediately.
The injection is a complex peptide delivered via prefilled multidose pens and indicated as an adjunct to diet and increased activity for chronic weight management. According to the company, IQVIA MAT Dec 2025 estimates the U.S. GLP‑1 weight‑management market at about USD 127 million.
Positive
- USFDA ANDA approval achieved by partner Orbicular for generic liraglutide
- Immediate U.S. launch with Cipla leading marketing and distribution
- Complex peptide offering expands Cipla's differentiated U.S. peptide portfolio
- Presence in GLP‑1 class alongside generic Victoza strengthens commercial positioning
- Addressable market ~USD 127M for GLP‑1 weight‑management (IQVIA MAT Dec 2025)
Negative
- None.
Partner Orbicular receives ANDA approval from USFDA
This milestone builds on the recent Abbreviated New Drug Approval (ANDA) by United States Food & Drugs Administration (USFDA) obtained by its partner, Orbicular, for Liraglutide Injection(generic Saxenda®). Cipla will lead the product's marketing and distribution, enabling broad access and reliable availability for patients. The company is set to commence the launch on an immediate basis.
Liraglutide Injection is a complex injectable peptide delivered through a multidose injector pen drug–device combination. It is indicated as an adjunct to a reduced–calorie diet and increased physical activity for chronic weight management in patients meeting defined clinical criteria.
Commenting on the launch, Achin Gupta, Global CEO & MD Designate, Cipla, said, "This development represents a key milestone in our peptide portfolio and strengthens our differentiated
Marc Falkin, CEO, Cipla North America, added: "We appreciate Orbicular's work in achieving FDA approval, which enables our immediate
GLP–1 receptor agonists have emerged as one of the fastest–growing therapeutic classes globally, driven by the rising prevalence of obesity and metabolic disorders, strong clinical outcomes, and increasing physician adoption.
According to IQVIA MAT December 2025, the total addressable market opportunity for GLP–1 therapies in weight management in the
About Glucagon–Like Peptide–1 (GLP–1)
Glucagon–like peptide–1 (GLP–1) therapies help regulate blood glucose levels and promote weight loss by enhancing insulin secretion, suppressing glucagon release, delaying gastric emptying, and reducing food intake—supporting improved metabolic control and weight management outcomes.
About Liraglutide
Liraglutide is a synthetic analog of the human GLP–1 hormone and is administered as a once–daily subcutaneous injection. The molecule was first approved for medical use in the European Union in 2009 and in
About Cipla Limited
Established in 1935, Cipla is a global pharmaceutical company focused on agile and sustainable growth, complex generics, and deepening portfolio in our home markets of
About Orbicular Pharmaceuticals, Inc.
Orbicular Pharmaceuticals Pharmaceutical Technologies Pvt. Ltd. Is a specialty pharmaceutical company focused on developing and securing regulatory approvals for technologically advanced, challenging products in complex generics. Orbicular is the ANDA holder for generic liraglutide injection.
Disclaimer
This press release contains forward–looking statements based on current expectations and beliefs of management. Actual results may differ materially due to risks and uncertainties, including market conditions, supply dynamics, and commercialization execution. Cipla undertakes no obligation to update any forward–looking statements.
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SOURCE Cipla USA Inc.