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
72189-298-20	72189-298	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET	ORAL	20211129	N/A	ANDA	ANDA210394	DirectRx	SILDENAFIL CITRATE	20 mg/1	20 TABLET in 1 BOTTLE (72189-298-20)
72189-298-30	72189-298	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET	ORAL	20220728	N/A	ANDA	ANDA210394	DirectRx	SILDENAFIL CITRATE	20 mg/1	30 TABLET in 1 BOTTLE (72189-298-30)
72189-298-90	72189-298	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET	ORAL	20211129	N/A	ANDA	ANDA210394	DirectRx	SILDENAFIL CITRATE	20 mg/1	90 TABLET in 1 BOTTLE (72189-298-90)
68788-7974-6	68788-7974	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20210728	N/A	ANDA	ANDA210394	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	20 mg/1	60 TABLET in 1 BOTTLE (68788-7974-6)
68788-7974-9	68788-7974	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20210728	N/A	ANDA	ANDA210394	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	20 mg/1	90 TABLET in 1 BOTTLE (68788-7974-9)
68788-7974-3	68788-7974	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20210728	N/A	ANDA	ANDA210394	Preferred Pharmaceuticals Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET in 1 BOTTLE (68788-7974-3)