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）
检索条件:" 注册申请号=ANDA202087"
符合检索条件的记录共 7 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
42806-662-05 42806-662 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (42806-662-05)
42806-663-01 42806-663 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (42806-663-01)
42806-663-05 42806-663 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (42806-663-05)
42806-664-01 42806-664 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 15 mg/1 100 TABLET in 1 BOTTLE (42806-664-01)
42806-664-05 42806-664 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 15 mg/1 500 TABLET in 1 BOTTLE (42806-664-05)
42806-665-60 42806-665 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 30 mg/1 60 TABLET in 1 BOTTLE (42806-665-60)
42806-662-01 42806-662 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20200619 N/A ANDA ANDA202087 EPIC PHARMA, LLC BUSPIRONE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (42806-662-01)
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