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
0093-7655-56	0093-7655	HUMAN PRESCRIPTION DRUG	Vardenafil Hydrochloride	Vardenafil Hydrochloride	TABLET, FILM COATED	ORAL	20190103	N/A	ANDA	ANDA091347	Teva Pharmaceuticals USA, Inc.	VARDENAFIL HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7655-56)
0093-7654-56	0093-7654	HUMAN PRESCRIPTION DRUG	Vardenafil Hydrochloride	Vardenafil Hydrochloride	TABLET, FILM COATED	ORAL	20190103	N/A	ANDA	ANDA091347	Teva Pharmaceuticals USA, Inc.	VARDENAFIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7654-56)
0093-7653-56	0093-7653	HUMAN PRESCRIPTION DRUG	Vardenafil Hydrochloride	Vardenafil Hydrochloride	TABLET, FILM COATED	ORAL	20190103	N/A	ANDA	ANDA091347	Teva Pharmaceuticals USA, Inc.	VARDENAFIL HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7653-56)
0093-7652-56	0093-7652	HUMAN PRESCRIPTION DRUG	Vardenafil Hydrochloride	Vardenafil Hydrochloride	TABLET, FILM COATED	ORAL	20190103	N/A	ANDA	ANDA091347	Teva Pharmaceuticals USA, Inc.	VARDENAFIL HYDROCHLORIDE	2.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-7652-56)
71335-9688-1	71335-9688	HUMAN PRESCRIPTION DRUG	Vardenafil Hydrochloride	Vardenafil Hydrochloride	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA091347	Bryant Ranch Prepack	VARDENAFIL HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-9688-1)