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
71205-509-30	71205-509	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201124	N/A	ANDA	ANDA078380	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-509-30)
71205-509-60	71205-509	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201124	N/A	ANDA	ANDA078380	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-509-60)
71205-509-90	71205-509	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20201124	N/A	ANDA	ANDA078380	Proficient Rx LP	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-509-90)
0093-5517-98	0093-5517	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20130531	N/A	ANDA	ANDA078380	Teva Pharmaceuticals USA, Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)
53002-1719-3	53002-1719	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20181001	N/A	ANDA	ANDA078380	RPK Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1719-3)
43063-668-30	43063-668	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20160415	N/A	ANDA	ANDA078380	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-668-30)