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
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)
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)
60219-1751-7	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)
60219-1752-1	60219-1752	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (60219-1752-1)
60219-1752-3	60219-1752	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60219-1752-3)
60219-1752-7	60219-1752	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180628	N/A	ANDA	ANDA202023	Amneal Pharmaceuticals NY LLC	SILDENAFIL CITRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60219-1752-7)
68071-2985-3	68071-2985	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20230417	N/A	ANDA	ANDA202023	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2985-3)