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
69238-1349-3	69238-1349	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 (69238-1349-3)
42291-864-30	42291-864	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20210121	N/A	ANDA	ANDA209744	AvKARE	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-864-30)
42291-865-30	42291-865	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20210121	N/A	ANDA	ANDA209744	AvKARE	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-865-30)
42291-866-30	42291-866	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20210121	N/A	ANDA	ANDA209744	AvKARE	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-866-30)
42291-867-30	42291-867	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20210121	N/A	ANDA	ANDA209744	AvKARE	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-867-30)