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
68382-898-99	68382-898	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	10 mg/1	2 BLISTER PACK in 1 CARTON (68382-898-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK
68382-899-01	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-899-01)
68382-899-05	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-899-05)
68382-899-06	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-899-06)
68382-899-10	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)
68382-899-16	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-899-16)
68382-899-99	68382-899	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	20 mg/1	2 BLISTER PACK in 1 CARTON (68382-899-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK
68382-896-05	68382-896	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	2.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-896-05)
68382-896-06	68382-896	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-896-06)
68382-896-10	68382-896	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190327	N/A	ANDA	ANDA206693	Zydus Pharmaceuticals USA Inc.	TADALAFIL	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-896-10)
51655-063-54	51655-063	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20220927	N/A	ANDA	ANDA206693	Northwind Pharmaceuticals, LLC	TADALAFIL	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-063-54)
51655-063-87	51655-063	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20220927	N/A	ANDA	ANDA206693	Northwind Pharmaceuticals, LLC	TADALAFIL	20 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-063-87)