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
76420-642-90	76420-642	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231031	N/A	ANDA	ANDA207244	Asclemed USA, Inc.	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-642-90)
76420-642-60	76420-642	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231031	N/A	ANDA	ANDA207244	Asclemed USA, Inc.	TADALAFIL	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-642-60)
76420-642-30	76420-642	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231031	N/A	ANDA	ANDA207244	Asclemed USA, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-642-30)
33342-265-07	33342-265	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191008	N/A	ANDA	ANDA207244	Macleods Pharmaceuticals Limited	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-265-07)
33342-266-07	33342-266	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191008	N/A	ANDA	ANDA207244	Macleods Pharmaceuticals Limited	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-266-07)
33342-267-07	33342-267	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191008	N/A	ANDA	ANDA207244	Macleods Pharmaceuticals Limited	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-267-07)
33342-268-07	33342-268	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20191008	N/A	ANDA	ANDA207244	Macleods Pharmaceuticals Limited	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-268-07)