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
71205-268-10	71205-268	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190701	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	20 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71205-268-10)
71205-268-30	71205-268	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-268-30)
71205-268-60	71205-268	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-268-60)
71205-268-90	71205-268	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190501	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-268-90)
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)
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)
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)