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
71205-088-60	71205-088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-088-60)
71205-088-90	71205-088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-088-90)
71205-088-30	71205-088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-088-30)
71205-088-50	71205-088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71205-088-50)
71205-088-10	71205-088	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20180801	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-088-10)