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
69097-373-94	69097-373	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	2.5 mg/1	2 BLISTER PACK in 1 CARTON (69097-373-94) / 15 TABLET, FILM COATED in 1 BLISTER PACK (69097-373-56)
69097-373-15	69097-373	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-373-15)
69097-373-05	69097-373	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-373-05)
69097-373-02	69097-373	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-373-02)
69097-374-02	69097-374	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-374-02)
69097-375-02	69097-375	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-375-02)
69097-375-05	69097-375	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-375-05)
69097-375-15	69097-375	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-375-15)
69097-376-02	69097-376	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69097-376-02)
69097-376-05	69097-376	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-376-05)
69097-376-15	69097-376	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-376-15)
69097-374-05	69097-374	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69097-374-05)
69097-374-15	69097-374	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69097-374-15)
69097-374-94	69097-374	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA209539	Cipla USA Inc.	TADALAFIL	5 mg/1	2 BLISTER PACK in 1 CARTON (69097-374-94) / 15 TABLET, FILM COATED in 1 BLISTER PACK (69097-374-56)
50090-5187-0	50090-5187	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200929	N/A	ANDA	ANDA209539	A-S Medication Solutions	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5187-0)
50090-5187-1	50090-5187	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200929	N/A	ANDA	ANDA209539	A-S Medication Solutions	TADALAFIL	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-5187-1)