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
72189-298-15	72189-298	HUMAN PRESCRIPTION DRUG	SILDENAFIL	SILDENAFIL	TABLET	ORAL	20211129	N/A	ANDA	ANDA210394	DirectRx	SILDENAFIL CITRATE	20 mg/1	15 TABLET in 1 BOTTLE (72189-298-15)
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)
70518-3433-2	70518-3433	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20220609	N/A	ANDA	ANDA210394	REMEDYREPACK INC.	SILDENAFIL CITRATE	20 mg/1	360 POUCH in 1 BOX (70518-3433-2) / 1 TABLET in 1 POUCH (70518-3433-1)
70518-3433-4	70518-3433	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20240110	N/A	ANDA	ANDA210394	REMEDYREPACK INC.	SILDENAFIL CITRATE	20 mg/1	180 POUCH in 1 BOX (70518-3433-4) / 1 TABLET in 1 POUCH (70518-3433-1)
68071-2602-3	68071-2602	HUMAN PRESCRIPTION DRUG	Sildenafil	Sildenafil	TABLET	ORAL	20211217	N/A	ANDA	ANDA210394	NuCare Pharmaceuticals,Inc.	SILDENAFIL CITRATE	20 mg/1	30 TABLET in 1 BOTTLE (68071-2602-3)