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
71610-074-60	71610-074	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20180521	N/A	ANDA	ANDA076214	Aphena Pharma Solutions - Tennessee, LLC	SOTALOL HYDROCHLORIDE	80 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71610-074-60)
71610-074-30	71610-074	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20180521	N/A	ANDA	ANDA076214	Aphena Pharma Solutions - Tennessee, LLC	SOTALOL HYDROCHLORIDE	80 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71610-074-30)
60505-0223-2	60505-0223	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	120 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (60505-0223-2)
60505-0224-1	60505-0224	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	160 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (60505-0224-1)
60505-0224-2	60505-0224	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	160 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (60505-0224-2)
60505-0222-2	60505-0222	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	80 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (60505-0222-2)
60505-0222-1	60505-0222	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (60505-0222-1)
60505-0223-1	60505-0223	HUMAN PRESCRIPTION DRUG	Sotalol Hydrochloride	Sotalol Hydrochloride	TABLET	ORAL	20030909	N/A	ANDA	ANDA076214	Apotex Corp.	SOTALOL HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (60505-0223-1)