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
43353-345-10	43353-345	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil citrate	TABLET, FILM COATED	ORAL	20170703	N/A	NDA AUTHORIZED GENERIC	NDA021845	Aphena Pharma Solutions - Tennessee, LLC	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (43353-345-10)
43353-345-20	43353-345	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil citrate	TABLET, FILM COATED	ORAL	20170703	N/A	NDA AUTHORIZED GENERIC	NDA021845	Aphena Pharma Solutions - Tennessee, LLC	SILDENAFIL CITRATE	20 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (43353-345-20)
43353-345-53	43353-345	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil citrate	TABLET, FILM COATED	ORAL	20170703	N/A	NDA AUTHORIZED GENERIC	NDA021845	Aphena Pharma Solutions - Tennessee, LLC	SILDENAFIL CITRATE	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (43353-345-53)
59762-0033-1	59762-0033	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20120927	20251231	NDA AUTHORIZED GENERIC	NDA021845	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (59762-0033-1)
59762-0033-3	59762-0033	HUMAN PRESCRIPTION DRUG	Sildenafil	sildenafil	TABLET, FILM COATED	ORAL	20201109	20260731	NDA AUTHORIZED GENERIC	NDA021845	Mylan Pharmaceuticals Inc.	SILDENAFIL CITRATE	20 mg/1	300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)
0069-4190-68	0069-4190	HUMAN PRESCRIPTION DRUG	Revatio	sildenafil citrate	TABLET, FILM COATED	ORAL	20050603	N/A	NDA	NDA021845	PFIZER LABORATORIES DIV PFIZER INC	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (0069-4190-68)