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
75834-250-30	75834-250	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (75834-250-30)
82804-041-60	82804-041	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-041-60)
82804-041-90	82804-041	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-041-90)
82804-041-30	82804-041	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20231213	N/A	ANDA	ANDA211298	Proficient Rx LP	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82804-041-30)
60290-027-01	60290-027	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60290-027-01)
60290-027-02	60290-027	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60290-027-02)
60290-027-03	60290-027	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (60290-027-03)
75834-249-01	75834-249	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (75834-249-01)
75834-249-10	75834-249	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (75834-249-10)
75834-249-30	75834-249	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (75834-249-30)
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)
60290-029-01	60290-029	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60290-029-01)
60290-029-02	60290-029	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60290-029-02)
60290-029-03	60290-029	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20260215	N/A	ANDA	ANDA211298	Umedica Laboratories USA Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (60290-029-03)
75834-247-01	75834-247	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (75834-247-01)
75834-247-15	75834-247	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (75834-247-15)
75834-247-30	75834-247	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA211298	NIVAGEN PHARMACEUTICALS, INC.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (75834-247-30)