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
67296-1488-9	67296-1488	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA204883	RedPharm Drug Inc	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (67296-1488-9)
51655-793-52	51655-793	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA204883	Northwind Pharmaceuticals	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-52)
71205-305-10	71205-305	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-305-10)
71205-305-20	71205-305	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-305-20)
71205-305-30	71205-305	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-305-30)
71205-305-60	71205-305	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-305-60)
71205-305-90	71205-305	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20190801	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-305-90)
51655-793-20	51655-793	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA204883	Northwind Pharmaceuticals	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20)
72888-018-00	72888-018	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20210305	N/A	ANDA	ANDA204883	Advagen Pharma Ltd	SILDENAFIL CITRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72888-018-00)
71205-623-10	71205-623	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20211229	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-623-10)
71205-623-30	71205-623	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20211123	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-623-30)
71205-623-60	71205-623	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20211123	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-623-60)
71205-623-90	71205-623	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20211123	N/A	ANDA	ANDA204883	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-623-90)
72888-018-90	72888-018	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20210305	N/A	ANDA	ANDA204883	Advagen Pharma Ltd	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72888-018-90)
52817-295-00	52817-295	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA204883	TruPharma LLC	SILDENAFIL CITRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)
52817-295-90	52817-295	HUMAN PRESCRIPTION DRUG	Sildenafil Citrate	Sildenafil	TABLET, FILM COATED	ORAL	20160801	N/A	ANDA	ANDA204883	TruPharma LLC	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)