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
43063-982-10	43063-982	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190808	N/A	ANDA	ANDA203963	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-982-10)
43063-982-30	43063-982	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA203963	PD-Rx Pharmaceuticals, Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-982-30)
65862-688-90	65862-688	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20151118	N/A	ANDA	ANDA203963	Aurobindo Pharma Limited	SILDENAFIL CITRATE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-688-90)
65862-688-99	65862-688	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET, FILM COATED	ORAL	20151118	N/A	ANDA	ANDA203963	Aurobindo Pharma Limited	SILDENAFIL CITRATE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-688-99)