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
72384-751-30	72384-751	HUMAN PRESCRIPTION DRUG	Stendra	avanafil	TABLET	ORAL	20131227	N/A	NDA	NDA202276	Metuchen Pharmaceuticals, LLC	AVANAFIL	50 mg/1	30 TABLET in 1 BOTTLE (72384-751-30)
72384-753-30	72384-753	HUMAN PRESCRIPTION DRUG	Stendra	avanafil	TABLET	ORAL	20131227	N/A	NDA	NDA202276	Metuchen Pharmaceuticals, LLC	AVANAFIL	200 mg/1	30 TABLET in 1 BOTTLE (72384-753-30)
72384-753-99	72384-753	HUMAN PRESCRIPTION DRUG	Stendra	avanafil	TABLET	ORAL	20200810	N/A	NDA	NDA202276	Metuchen Pharmaceuticals, LLC	AVANAFIL	200 mg/1	6 BLISTER PACK in 1 CARTON (72384-753-99) / 1 TABLET in 1 BLISTER PACK (72384-753-01)
72384-752-30	72384-752	HUMAN PRESCRIPTION DRUG	Stendra	avanafil	TABLET	ORAL	20131227	N/A	NDA	NDA202276	Metuchen Pharmaceuticals, LLC	AVANAFIL	100 mg/1	30 TABLET in 1 BOTTLE (72384-752-30)
72384-752-99	72384-752	HUMAN PRESCRIPTION DRUG	Stendra	avanafil	TABLET	ORAL	20200810	N/A	NDA	NDA202276	Metuchen Pharmaceuticals, LLC	AVANAFIL	100 mg/1	6 BLISTER PACK in 1 CARTON (72384-752-99) / 1 TABLET in 1 BLISTER PACK (72384-752-01)