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
82804-042-60	82804-042	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231218	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-042-60)
82804-042-90	82804-042	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231218	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-042-90)
72789-407-30	72789-407	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA211298	PD-Rx Pharmaceuticals, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-407-30)
72789-407-90	72789-407	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240611	N/A	ANDA	ANDA211298	PD-Rx Pharmaceuticals, Inc.	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-407-90)
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)