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
71205-267-30	71205-267	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-267-30)
71205-267-60	71205-267	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-267-60)
71205-267-90	71205-267	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA077342	Proficient Rx LP	SILDENAFIL CITRATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-267-90)
0093-5343-01	0093-5343	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20171211	N/A	ANDA	ANDA077342	Teva Pharmaceuticals USA, Inc.	SILDENAFIL CITRATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-5343-01)
0093-5343-56	0093-5343	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20171211	N/A	ANDA	ANDA077342	Teva Pharmaceuticals USA, Inc.	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-5343-56)