SSY Group Receives NMPA Approval for Furosemide as API in Marketed Formulations

Stock News04-21

SSY GROUP (02005) announced that its Furosemide has been approved by the National Medical Products Administration (NMPA) for registration as an active pharmaceutical ingredient (API) intended for use in marketed drug formulations. As previously disclosed in the Company's announcements dated June 30, 2025, and December 27, 2024, the Group had already obtained drug production registration approvals from the NMPA for Furosemide Tablets and Furosemide Injection. Furosemide is primarily used to treat various edematous conditions, hypertension, hyperkalemia, hypercalcemia, dilutional hyponatremia, syndrome of inappropriate antidiuretic hormone secretion (SIADH), and acute drug or toxin poisoning (such as barbiturate poisoning), as well as for the prevention of acute renal failure.

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