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
63629-5029-3	63629-5029	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20130802	N/A	ANDA	ANDA202025	Bryant Ranch Prepack	SILDENAFIL CITRATE	20 mg/1	7 TABLET in 1 BOTTLE (63629-5029-3)
51655-172-20	51655-172	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20230419	N/A	ANDA	ANDA202025	Northwind Health Company, LLC	SILDENAFIL CITRATE	20 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-172-20)
51655-172-52	51655-172	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20230419	N/A	ANDA	ANDA202025	Northwind Health Company, LLC	SILDENAFIL CITRATE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-172-52)
53746-351-90	53746-351	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20121108	N/A	ANDA	ANDA202025	Amneal Pharmaceuticals of New York LLC	SILDENAFIL CITRATE	20 mg/1	90 TABLET in 1 BOTTLE (53746-351-90)