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
72162-1931-1	72162-1931	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20200724	N/A	ANDA	ANDA075563	Bryant Ranch Prepack	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE (72162-1931-1)
69584-842-10	69584-842	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20200724	N/A	ANDA	ANDA075563	Oxford Pharmaceuticals, LLC	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE (69584-842-10)
69584-842-30	69584-842	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20200724	N/A	ANDA	ANDA075563	Oxford Pharmaceuticals, LLC	SOTALOL HYDROCHLORIDE	120 mg/1	300 TABLET in 1 BOTTLE (69584-842-30)
43353-616-30	43353-616	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20100310	N/A	ANDA	ANDA075563	Aphena Pharma Solutions - Tennessee, LLC	SOTALOL HYDROCHLORIDE	80 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43353-616-30)
43353-616-60	43353-616	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20100310	N/A	ANDA	ANDA075563	Aphena Pharma Solutions - Tennessee, LLC	SOTALOL HYDROCHLORIDE	80 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (43353-616-60)
72789-137-01	72789-137	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20201106	N/A	ANDA	ANDA075563	PD-Rx Pharmaceuticals, Inc.	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72789-137-01)
63629-2423-1	63629-2423	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20200724	N/A	ANDA	ANDA075563	Bryant Ranch Prepack	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE (63629-2423-1)