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Basic Info

  • Grade: Pharmaceutical Grade

    Factory Location: Quanzhou

    Main Sales Markets: North America,Central/South America,Western Europe,Eastern Europe,Australasia,Asia,Middle East,Africa

  • Sample Provided: no

    Payment Terms: L/C

    On September 20, 2019, the FDA officially approved the marketing application of semaglutide for improving blood sugar control in patients with type 2 diabetes in combination with diet and exercise. Semaglutide is a human GLP-1 analogue with high albumin affinity and a long half-life, enabling once-weekly administration to stimulate insulin secretion and inhibit glucagon secretion in a blood sugar-dependent manner.

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    Quanzhou Fortune Biopharma Co.,Ltd.
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