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
71205-502-30	71205-502	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201111	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-502-30)
71205-720-04	71205-720	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20221116	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	10 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (71205-720-04)
71205-502-60	71205-502	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201111	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-502-60)
71205-502-90	71205-502	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20201111	N/A	ANDA	ANDA209167	Proficient Rx LP	TADALAFIL	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-502-90)
76420-126-15	76420-126	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20220129	N/A	ANDA	ANDA209167	Asclemed USA, Inc.	TADALAFIL	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (76420-126-15)
76420-126-30	76420-126	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA209167	Asclemed USA, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-126-30)
76420-126-90	76420-126	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA209167	Asclemed USA, Inc.	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-126-90)