Shanghai Fosun Pharmaceutical (Group) Co., Ltd. (“Fosun Pharma”) reported that its subsidiary, Fosun Wanbang (Jiangsu) Pharmaceutical Group, has received marketing authorisation from China’s National Medical Products Administration for Empagliflozin and Metformin Hydrochloride Sustained-release Tablets (III).
The dual-therapy tablet, containing 12.5 mg of empagliflozin and 1,000 mg of metformin hydrochloride, is approved as an adjunct to diet and exercise to improve glycaemic control in adult patients with type 2 diabetes mellitus already treated with both active ingredients. The product is registered as a Category 3 chemical drug under approval number “Guo Yao Zhun Zi H20265383.”
Fosun Pharma has invested a cumulative RMB 17.92 million in the drug’s development as of June 2026. Market data from IQVIA CHPA indicate that sales of comparable metformin–empagliflozin combinations in mainland China reached roughly RMB 674.00 million in 2025, underscoring the segment’s commercial relevance.
Management noted that the new approval broadens Fosun Pharma’s chronic-disease portfolio, though future sales will depend on factors such as prescription demand, competitive dynamics and distribution coverage.
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