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
71205-220-60	71205-220	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA203962	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60)
71205-220-90	71205-220	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA203962	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)
65862-689-01	65862-689	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA203962	Aurobindo Pharma Limited	SILDENAFIL CITRATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-689-01)
65862-689-05	65862-689	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20230710	N/A	ANDA	ANDA203962	Aurobindo Pharma Limited	SILDENAFIL CITRATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-689-05)
65862-689-30	65862-689	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA203962	Aurobindo Pharma Limited	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (65862-689-30)
65862-689-99	65862-689	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA203962	Aurobindo Pharma Limited	SILDENAFIL CITRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-689-99)