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
46708-234-30	46708-234	HUMAN PRESCRIPTION DRUG	VILAZODONE HYDROCHLORIDE	VILAZODONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220604	N/A	ANDA	ANDA208202	Alembic Pharmaceuticals Limited	VILAZODONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-234-30)
46708-234-71	46708-234	HUMAN PRESCRIPTION DRUG	VILAZODONE HYDROCHLORIDE	VILAZODONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220604	N/A	ANDA	ANDA208202	Alembic Pharmaceuticals Limited	VILAZODONE HYDROCHLORIDE	40 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (46708-234-71)
46708-234-90	46708-234	HUMAN PRESCRIPTION DRUG	VILAZODONE HYDROCHLORIDE	VILAZODONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220604	N/A	ANDA	ANDA208202	Alembic Pharmaceuticals Limited	VILAZODONE HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-234-90)
46708-234-91	46708-234	HUMAN PRESCRIPTION DRUG	VILAZODONE HYDROCHLORIDE	VILAZODONE HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20220604	N/A	ANDA	ANDA208202	Alembic Pharmaceuticals Limited	VILAZODONE HYDROCHLORIDE	40 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (46708-234-91)