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
31722-776-32	31722-776	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20141126	N/A	ANDA	ANDA203623	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-32)
72865-105-90	72865-105	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190710	N/A	ANDA	ANDA203623	XLCare Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72865-105-90)
31722-776-33	31722-776	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20141126	N/A	ANDA	ANDA203623	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-33)
31722-776-34	31722-776	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20141126	N/A	ANDA	ANDA203623	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-776-34)
31722-776-90	31722-776	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20141126	N/A	ANDA	ANDA203623	Camber Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-776-90)