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
82804-040-90	82804-040	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231110	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-040-90)
75834-248-01	75834-248	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (75834-248-01)
75834-248-15	75834-248	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (75834-248-15)
75834-248-30	75834-248	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (75834-248-30)
72789-408-30	72789-408	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240611	N/A	ANDA	ANDA211298	PD-Rx Pharmaceuticals, Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-30)
72789-408-90	72789-408	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240611	N/A	ANDA	ANDA211298	PD-Rx Pharmaceuticals, Inc.	TADALAFIL	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-408-90)