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
13668-188-10	13668-188	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA091448	Torrent Pharmaceuticals Limited	SILDENAFIL CITRATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (13668-188-10)
13668-188-30	13668-188	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA091448	Torrent Pharmaceuticals Limited	SILDENAFIL CITRATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-188-30)
13668-186-10	13668-186	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20241206	N/A	ANDA	ANDA091448	Torrent Pharmaceuticals Limited	SILDENAFIL CITRATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (13668-186-10)
13668-186-01	13668-186	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA091448	Torrent Pharmaceuticals Limited	SILDENAFIL CITRATE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13668-186-01)
13668-186-30	13668-186	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20180611	N/A	ANDA	ANDA091448	Torrent Pharmaceuticals Limited	SILDENAFIL CITRATE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (13668-186-30)
51655-794-54	51655-794	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA091448	Northwind Pharmaceuticals, LLC	SILDENAFIL CITRATE	100 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-794-54)
51655-794-87	51655-794	HUMAN PRESCRIPTION DRUG	SILDENAFIL CITRATE	SILDENAFIL	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA091448	Northwind Pharmaceuticals, LLC	SILDENAFIL CITRATE	100 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-794-87)