美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
76385-125-01	76385-125	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tables AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-125-01)
76385-125-50	76385-125	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tables AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	80 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-125-50)
76385-126-01	76385-126	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tables AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-126-01)
76385-126-50	76385-126	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tables AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	120 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-126-50)
76385-127-01	76385-127	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tablets AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	160 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-127-01)
76385-127-50	76385-127	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride AF	Sotalol Hydrochloride Tablets AF	TABLET	ORAL	20200221	N/A	ANDA	ANDA207429	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	160 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-127-50)