SSY Group (02005.HK): Diltiazem Hydrochloride for Injection and Propranolol Hydrochloride Injection Obtain Drug Production Registration Approvals

NewTimeSpace News: SSY Group Limited (02005.HK) announced that the Group has obtained the drug production registration approval issued by the National Medical Products Administration (NMPA) for Diltiazem Hydrochloride for Injection (10mg). Classified as a Class 4 chemical drug, it is deemed to have passed the consistency evaluation. Meanwhile, the Group has also secured registration approval for Propranolol Hydrochloride Injection (specifications: 5ml:5mg and 2ml:2mg). As a Class 3 chemical drug, it is also recognised as passing the consistency evaluation.

NewTimeSpace News: SSY Group Limited (02005.HK) released a voluntary announcement on April 27, 2026. The Group has been granted the drug production registration approval by the NMPA for Diltiazem Hydrochloride for Injection (10mg). Falling into the category of Class 4 chemical drugs, the product is deemed to have completed the generic consistency evaluation. It is mainly indicated for supraventricular tachycardia, emergency management of intraoperative hypertension, hypertensive emergencies and unstable angina.

In addition, the Group obtained NMPA production registration approval for Propranolol Hydrochloride Injection (5ml:5mg & 2ml:2mg), a Class 3 chemical drug with deemed consistency evaluation clearance. This product is widely used to control supraventricular and ventricular arrhythmias, effort angina, and phaeochromocytoma (combined withα-blockers for tachycardia management.

Previously, the Group’s propranolol hydrochloride active pharmaceutical ingredient (API) has been officially registered and approved by the NMPA for use in marketed pharmaceutical preparations.

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