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
60505-4372-3	60505-4372	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20231026	N/A	ANDA	ANDA208228	Apotex Corp.	VILAZODONE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (60505-4372-3)
60505-4373-3	60505-4373	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20231026	N/A	ANDA	ANDA208228	Apotex Corp.	VILAZODONE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (60505-4373-3)
60505-4374-3	60505-4374	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20231026	N/A	ANDA	ANDA208228	Apotex Corp.	VILAZODONE HYDROCHLORIDE	40 mg/1	30 TABLET in 1 BOTTLE (60505-4374-3)
72205-260-30	72205-260	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20230714	N/A	ANDA	ANDA208228	Novadoz Pharmaceuticals LLC	VILAZODONE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (72205-260-30)
72205-261-30	72205-261	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20230714	N/A	ANDA	ANDA208228	Novadoz Pharmaceuticals LLC	VILAZODONE HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE (72205-261-30)
72205-262-30	72205-262	HUMAN PRESCRIPTION DRUG	vilazodone hydrochloride	vilazodone hydrochloride	TABLET	ORAL	20230714	N/A	ANDA	ANDA208228	Novadoz Pharmaceuticals LLC	VILAZODONE HYDROCHLORIDE	40 mg/1	30 TABLET in 1 BOTTLE (72205-262-30)