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
76385-114-01	76385-114	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171215	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-114-01)
76385-114-50	76385-114	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171215	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	80 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-114-50)
76385-115-01	76385-115	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171215	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-115-01)
76385-115-50	76385-115	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171206	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	120 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-115-50)
76385-116-01	76385-116	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171206	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	160 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76385-116-01)
76385-116-50	76385-116	HUMAN PRESCRIPTION DRUG	Sotalol	Sotalol Hydrochloride	TABLET	ORAL	20171206	N/A	ANDA	ANDA207428	Bayshore Pharmaceuticals LLC	SOTALOL HYDROCHLORIDE	160 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (76385-116-50)