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
71610-603-08	71610-603	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	5 mg/1	8 TABLET, FILM COATED in 1 BOTTLE (71610-603-08)
71610-603-11	71610-603	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	5 mg/1	48 TABLET, FILM COATED in 1 BOTTLE (71610-603-11)
71610-603-23	71610-603	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211018	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	5 mg/1	16 TABLET, FILM COATED in 1 BOTTLE (71610-603-23)
71610-603-36	71610-603	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240322	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	5 mg/1	2940 TABLET, FILM COATED in 1 BOTTLE (71610-603-36)
60219-1349-3	60219-1349	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA209744	Amneal Pharmaceuticals NY LLC	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60219-1349-3)