Nimodipine API Approved by Shijiazhuang Sihua Pharmaceutical Group
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TIME:2025-03-19

On March 19, the nimodipine active pharmaceutical ingredient developed by Hebei Guangxiang Pharmaceutical Co., Ltd., a subsidiary of Shijiazhuang Sihua Pharmaceutical Group, was approved for registration by the National Medical Products Administration and officially listed as an API used in marketed dosage forms. This marks another “dihydropyridine” class antihypertensive API to receive approval, following the 2025 approvals for benidipine hydrochloride and nicardipine hydrochloride APIs.
To date, the Group has cumulatively obtained approval for 71 bulk and specialty API varieties, with Guangxiang Pharmaceutical securing approval for 40 new API products.
According to available information, nimodipine is a second-generation dihydropyridine calcium channel blocker, primarily indicated for the treatment of ischemic cerebrovascular diseases, migraine, sudden sensorineural hearing loss, mild to moderate hypertension, and the prevention of cerebral vasospasm following mild subarachnoid hemorrhage, as well as for the management of age-related cognitive impairment.
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