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
71610-581-06	71610-581	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230201	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	10 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-06)
71610-581-12	71610-581	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20210712	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	10 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-581-12)
71610-581-39	71610-581	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	10 mg/1	1440 TABLET, FILM COATED in 1 BOTTLE (71610-581-39)
71610-581-52	71610-581	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240905	N/A	ANDA	ANDA209744	Aphena Pharma Solutions - Tennessee, LLC	TADALAFIL	10 mg/1	18 TABLET, FILM COATED in 1 BOTTLE (71610-581-52)
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)