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
63629-8409-2	63629-8409	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20220614	N/A	ANDA	ANDA209167	Bryant Ranch Prepack	TADALAFIL	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-8409-2)
63629-8409-3	63629-8409	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20241029	N/A	ANDA	ANDA209167	Bryant Ranch Prepack	TADALAFIL	2.5 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63629-8409-3)
51655-473-54	51655-473	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201106	N/A	ANDA	ANDA209167	Northwind Health Company, LLC	TADALAFIL	20 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-473-54)
51655-473-87	51655-473	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201106	N/A	ANDA	ANDA209167	Northwind Health Company, LLC	TADALAFIL	20 mg/1	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-473-87)
63629-8409-4	63629-8409	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20241029	N/A	ANDA	ANDA209167	Bryant Ranch Prepack	TADALAFIL	2.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63629-8409-4)
68071-2553-3	68071-2553	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211025	N/A	ANDA	ANDA209167	NuCare Pharmaceuticals,Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2553-3)
68788-8153-7	68788-8153	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20220314	N/A	ANDA	ANDA209167	Preferred Pharmaceuticals Inc.	TADALAFIL	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (68788-8153-7)