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
71205-418-30	71205-418	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200304	N/A	ANDA	ANDA090141	Proficient Rx LP	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-418-30)
71205-418-60	71205-418	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200304	N/A	ANDA	ANDA090141	Proficient Rx LP	TADALAFIL	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-418-60)
71205-418-90	71205-418	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200304	N/A	ANDA	ANDA090141	Proficient Rx LP	TADALAFIL	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-418-90)
0093-3018-56	0093-3018	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20180927	20250131	ANDA	ANDA090141	Teva Pharmaceuticals USA, Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3018-56)
0093-3019-56	0093-3019	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20180927	20250131	ANDA	ANDA090141	Teva Pharmaceuticals USA, Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3019-56)
0093-3017-65	0093-3017	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20180927	N/A	ANDA	ANDA090141	Teva Pharmaceuticals USA, Inc.	TADALAFIL	5 mg/1	2 BLISTER PACK in 1 BOX (0093-3017-65) / 15 TABLET, FILM COATED in 1 BLISTER PACK (0093-3017-30)
0093-3017-56	0093-3017	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20180927	20250131	ANDA	ANDA090141	Teva Pharmaceuticals USA, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3017-56)
0093-3016-65	0093-3016	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20180927	N/A	ANDA	ANDA090141	Teva Pharmaceuticals USA, Inc.	TADALAFIL	2.5 mg/1	2 BLISTER PACK in 1 BOX (0093-3016-65) / 15 TABLET, FILM COATED in 1 BLISTER PACK (0093-3016-30)