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
50090-6649-0	50090-6649	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20230830	N/A	ANDA	ANDA075388	A-S Medication Solutions	BUSPIRONE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (50090-6649-0)
69584-093-06	69584-093	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20250824	N/A	ANDA	ANDA075388	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	15 mg/1	60 TABLET in 1 BOTTLE (69584-093-06)
69584-093-10	69584-093	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200727	N/A	ANDA	ANDA075388	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	15 mg/1	100 TABLET in 1 BOTTLE (69584-093-10)
69584-092-50	69584-092	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200727	N/A	ANDA	ANDA075388	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	10 mg/1	500 TABLET in 1 BOTTLE (69584-092-50)
69584-093-50	69584-093	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200727	N/A	ANDA	ANDA075388	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	15 mg/1	500 TABLET in 1 BOTTLE (69584-093-50)
70518-2987-0	70518-2987	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20210112	N/A	ANDA	ANDA075388	REMEDYREPACK INC.	BUSPIRONE HYDROCHLORIDE	15 mg/1	30 TABLET in 1 BLISTER PACK (70518-2987-0)
70518-2987-2	70518-2987	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20250712	N/A	ANDA	ANDA075388	REMEDYREPACK INC.	BUSPIRONE HYDROCHLORIDE	15 mg/1	60 TABLET in 1 BLISTER PACK (70518-2987-2)