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
0093-1063-01	0093-1063	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20000505	N/A	ANDA	ANDA075429	Teva Pharmaceuticals USA, Inc.	SOTALOL HYDROCHLORIDE	240 mg/1	100 TABLET in 1 BOTTLE (0093-1063-01)
71205-046-30	71205-046	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20180601	N/A	ANDA	ANDA075429	Proficient Rx LP	SOTALOL HYDROCHLORIDE	80 mg/1	30 TABLET in 1 BOTTLE (71205-046-30)
71205-046-60	71205-046	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20180601	N/A	ANDA	ANDA075429	Proficient Rx LP	SOTALOL HYDROCHLORIDE	80 mg/1	60 TABLET in 1 BOTTLE (71205-046-60)
71205-046-90	71205-046	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20180601	N/A	ANDA	ANDA075429	Proficient Rx LP	SOTALOL HYDROCHLORIDE	80 mg/1	90 TABLET in 1 BOTTLE (71205-046-90)
0093-1062-01	0093-1062	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20000505	N/A	ANDA	ANDA075429	Teva Pharmaceuticals USA, Inc.	SOTALOL HYDROCHLORIDE	160 mg/1	100 TABLET in 1 BOTTLE (0093-1062-01)
0093-1061-01	0093-1061	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20000504	N/A	ANDA	ANDA075429	Teva Pharmaceuticals USA, Inc.	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE (0093-1061-01)
0093-1060-01	0093-1060	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20000505	N/A	ANDA	ANDA075429	Teva Pharmaceuticals USA, Inc.	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE (0093-1060-01)