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
50090-6804-0	50090-6804	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20231106	N/A	ANDA	ANDA204882	A-S Medication Solutions	SILDENAFIL CITRATE	50 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-6804-0)
72888-016-00	72888-016	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20211108	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72888-016-00)
72888-016-30	72888-016	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20210617	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72888-016-30)
72888-017-00	72888-017	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20211108	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72888-017-00)
72888-017-01	72888-017	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20210617	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72888-017-01)
72888-017-30	72888-017	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20210617	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72888-017-30)
72888-015-30	72888-015	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20210617	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72888-015-30)
72888-015-05	72888-015	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20211108	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72888-015-05)
72888-016-01	72888-016	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20210617	N/A	ANDA	ANDA204882	Advagen Pharma Ltd	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72888-016-01)
52817-340-30	52817-340	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20180701	N/A	ANDA	ANDA204882	TruPharma LLC	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (52817-340-30)
52817-342-30	52817-342	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20180701	N/A	ANDA	ANDA204882	TruPharma LLC	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (52817-342-30)
52817-341-10	52817-341	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20180701	N/A	ANDA	ANDA204882	TruPharma LLC	SILDENAFIL CITRATE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (52817-341-10)
52817-341-30	52817-341	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20180701	N/A	ANDA	ANDA204882	TruPharma LLC	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (52817-341-30)
52817-342-10	52817-342	HUMAN PRESCRIPTION DRUG	SILDENAFIL	sildenafil	TABLET, FILM COATED	ORAL	20180701	N/A	ANDA	ANDA204882	TruPharma LLC	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (52817-342-10)