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
47335-010-83	47335-010	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA208934	Sun Pharmaceutical Industries, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-010-83)
47335-011-83	47335-011	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA208934	Sun Pharmaceutical Industries, Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-011-83)
47335-012-83	47335-012	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20190326	N/A	ANDA	ANDA208934	Sun Pharmaceutical Industries, Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-012-83)
76420-541-30	76420-541	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230314	N/A	ANDA	ANDA208934	Asclemed USA, Inc.	TADALAFIL	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-541-30)
76420-541-90	76420-541	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230314	N/A	ANDA	ANDA208934	Asclemed USA, Inc.	TADALAFIL	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-541-90)
76420-542-30	76420-542	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230314	N/A	ANDA	ANDA208934	Asclemed USA, Inc.	TADALAFIL	2.5 mg/1	2 BLISTER PACK in 1 CARTON (76420-542-30) / 15 TABLET, FILM COATED in 1 BLISTER PACK
76420-543-30	76420-543	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20230314	N/A	ANDA	ANDA208934	Asclemed USA, Inc.	TADALAFIL	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-543-30)
76420-544-30	76420-544	HUMAN PRESCRIPTION DRUG	Tadalafil	Tadalafil	TABLET, FILM COATED	ORAL	20200219	N/A	ANDA	ANDA208934	Asclemed USA, Inc.	TADALAFIL	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-544-30)