2025 年 12 月 9 日，翼思生物旗下药品盐酸索安非托片（Solriamfetol Hydrochloride Tablets，翼朗清 ® ）正式获中国国家药品监督管理局（NMPA）批准，用于改善阻塞性睡眠呼吸暂停（OSA）伴有日间过度嗜睡（EDS）的成人患者的觉醒程度 [1,2] 。作为一款全新的多巴胺和去甲 ...

HYDERABAD, India & PRINCETON, N.J.--(BUSINESS WIRE)--Dr. Reddy’s Laboratories Ltd. (BSE: 500124, NSE: DRREDDY, NYSE: RDY, along with its subsidiaries together referred to as “Dr. Reddy’s”) today ...

Zydus Lifesciences Limited has received final approval from the United States Food and Drug Administration (FDA) for verapamil hydrochloride extended-release tablets USP, 120 mg, 180 mg and 240 mg ...

PRINCETON, N.J., Dec. 31 /PRNewswire/ -- Ranbaxy Laboratories Limited (RLL), announced today that the company has received final approval from the U.S. Food and Drug Administration to manufacture and ...

Lupin has received tentative approval from the Food and Drug Administration for sitagliptin and metformin hydrochloride tablets, 50 mg/500 mg and 50 mg/1000 mg, which is a generic of Merck Sharp & ...

The recall involves Lot# GMML24026A (NDC# 29300-415-19) with an expiration date of September 2027. Unichem Pharmaceuticals is recalling 1 lot of Cyclobenzaprine Hydrochloride Tablets USP, 10mg due to ...