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
43598-578-30	43598-578	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190205	N/A	ANDA	ANDA210145	Dr.Reddys Laboratories Inc	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (43598-578-30)
43598-578-60	43598-578	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190205	N/A	ANDA	ANDA210145	Dr.Reddys Laboratories Inc	TADALAFIL	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (43598-578-60)
70518-2862-0	70518-2862	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200826	N/A	ANDA	ANDA210145	REMEDYREPACK INC.	TADALAFIL	20 mg/1	12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2862-0)
70518-2862-1	70518-2862	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20211209	N/A	ANDA	ANDA210145	REMEDYREPACK INC.	TADALAFIL	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2862-1)