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
71335-0969-6	71335-0969	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181128	N/A	ANDA	ANDA202023	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0969-6)
71335-0969-7	71335-0969	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240517	N/A	ANDA	ANDA202023	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71335-0969-7)
71335-0969-8	71335-0969	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240517	N/A	ANDA	ANDA202023	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0969-8)
71335-0969-9	71335-0969	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20240517	N/A	ANDA	ANDA202023	Bryant Ranch Prepack	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0969-9)
60219-1751-7	60219-1751	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60219-1751-7)
60219-1751-3	60219-1751	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60219-1751-3)
60219-1751-1	60219-1751	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60219-1751-1)