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
70518-3529-0	70518-3529	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200920	N/A	ANDA	ANDA207290	REMEDYREPACK INC.	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3529-0)
70518-3529-1	70518-3529	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230707	N/A	ANDA	ANDA207290	REMEDYREPACK INC.	TADALAFIL	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3529-1)
33342-278-07	33342-278	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191030	N/A	ANDA	ANDA207290	Macleods Pharmaceuticals Limited	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-278-07)
33342-278-09	33342-278	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191030	N/A	ANDA	ANDA207290	Macleods Pharmaceuticals Limited	TADALAFIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (33342-278-09)