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
0480-2308-65	0480-2308	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20241106	20260131	ANDA	ANDA205885	Teva Pharmaceuticals, Inc.	TADALAFIL	2.5 mg/1	2 BLISTER PACK in 1 CARTON (0480-2308-65) / 15 TABLET, FILM COATED in 1 BLISTER PACK (0480-2308-30)
0480-2311-56	0480-2311	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240116	N/A	ANDA	ANDA205885	Teva Pharmaceuticals, Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0480-2311-56)
0480-2309-56	0480-2309	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240116	N/A	ANDA	ANDA205885	Teva Pharmaceuticals, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0480-2309-56)
0480-2309-65	0480-2309	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20241106	20260228	ANDA	ANDA205885	Teva Pharmaceuticals, Inc.	TADALAFIL	5 mg/1	2 BLISTER PACK in 1 CARTON (0480-2309-65) / 15 TABLET, FILM COATED in 1 BLISTER PACK (0480-2309-30)
0480-2310-56	0480-2310	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20240207	N/A	ANDA	ANDA205885	Teva Pharmaceuticals, Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0480-2310-56)