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
63629-2415-1	63629-2415	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20210224	N/A	ANDA	ANDA078302	Bryant Ranch Prepack	BUSPIRONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE (63629-2415-1)
63629-2414-1	63629-2414	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20210224	N/A	ANDA	ANDA078302	Bryant Ranch Prepack	BUSPIRONE HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (63629-2414-1)
69584-094-18	69584-094	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200501	N/A	ANDA	ANDA078302	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	30 mg/1	180 TABLET in 1 BOTTLE (69584-094-18)
69584-094-06	69584-094	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200501	N/A	ANDA	ANDA078302	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE (69584-094-06)
69584-094-50	69584-094	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200501	N/A	ANDA	ANDA078302	Oxford Pharmaceuticals, LLC	BUSPIRONE HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (69584-094-50)
72162-1927-5	72162-1927	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200501	N/A	ANDA	ANDA078302	Bryant Ranch Prepack	BUSPIRONE HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (72162-1927-5)
72162-1927-6	72162-1927	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20200501	N/A	ANDA	ANDA078302	Bryant Ranch Prepack	BUSPIRONE HYDROCHLORIDE	30 mg/1	60 TABLET in 1 BOTTLE (72162-1927-6)
72789-142-01	72789-142	HUMAN PRESCRIPTION DRUG	Buspirone Hydrochloride	buspirone hydrochloride	TABLET	ORAL	20201106	N/A	ANDA	ANDA078302	PD-Rx Pharmaceuticals, Inc.	BUSPIRONE HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72789-142-01)