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
24658-771-01	24658-771	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20161114	N/A	ANDA	ANDA072711	PuraCap Laboratories LLC dba Blu Pharmaceuticals	SULINDAC	200 mg/1	100 TABLET in 1 BOTTLE (24658-771-01)
24658-771-05	24658-771	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20161114	N/A	ANDA	ANDA072711	PuraCap Laboratories LLC dba Blu Pharmaceuticals	SULINDAC	200 mg/1	500 TABLET in 1 BOTTLE (24658-771-05)
42806-011-01	42806-011	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20100125	N/A	ANDA	ANDA072711	Epic Pharma, LLC	SULINDAC	200 mg/1	100 TABLET in 1 BOTTLE (42806-011-01)
42806-011-05	42806-011	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20100125	N/A	ANDA	ANDA072711	Epic Pharma, LLC	SULINDAC	200 mg/1	500 TABLET in 1 BOTTLE (42806-011-05)
42806-011-10	42806-011	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20100125	N/A	ANDA	ANDA072711	Epic Pharma, LLC	SULINDAC	200 mg/1	1000 TABLET in 1 BOTTLE (42806-011-10)
71205-648-30	71205-648	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20220328	N/A	ANDA	ANDA072711	Proficient Rx LP	SULINDAC	200 mg/1	30 TABLET in 1 BOTTLE (71205-648-30)
71205-648-60	71205-648	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20220328	N/A	ANDA	ANDA072711	Proficient Rx LP	SULINDAC	200 mg/1	60 TABLET in 1 BOTTLE (71205-648-60)
71205-648-90	71205-648	HUMAN PRESCRIPTION DRUG	SULINDAC	SULINDAC	TABLET	ORAL	20220328	N/A	ANDA	ANDA072711	Proficient Rx LP	SULINDAC	200 mg/1	90 TABLET in 1 BOTTLE (71205-648-90)