Lupin gets approval to launch flu medicine in China, enters Chinese market for first time

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Global pharmaceutical major Lupin Limited on Friday announced that China’s National Medical Products Administration has approved its Abbreviated New Drug Application for Oseltamivir Phosphate for oral suspension, developed in partnership with Yabao Pharmaceuticals.

The approval marks Lupin’s first product entry into the Chinese market, representing a development in the company’s global expansion plans.

Oseltamivir Phosphate for oral suspension, 6 mg/mL, will be launched and commercialised in China to expand access to influenza treatment and prevention, particularly for paediatric use.

Lupin said the approval reinforces its commitment to delivering high-quality and affordable medicines to patients and children in need.

The oral suspension is indicated for the treatment of influenza A and B in patients aged two weeks and older, and for the prevention of influenza A and B in individuals aged one year and above.

Fabrice Egros, President – Corporate Development, Lupin, said, “We are delighted that we have received approval for Oseltamivir Oral Suspension in China. This is a strategic step in our entry into one of the world’s largest pharmaceutical markets.”

He added that it reflects their shared commitment to expanding access to high-quality, affordable therapies, particularly in paediatric care.

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Wei Ren, President, Yabao, said, “We are pleased to announce the official approval of Oseltamivir Oral Suspension in China, marking a key milestone in our partnership with Lupin. It reinforces Yabao’s dedication to quality paediatric medicines and showcases our strong collaboration. We will further expand our R&D portfolio for paediatric and adult chronic disease drugs to jointly advance our businesses.”

Lupin Limited shares ended lower on Friday at ₹2,270.70 on the NSE, down ₹13.80 or 0.60% from the previous close.

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