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=ANDA075022"
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
71205-799-90 71205-799 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20230505 N/A ANDA ANDA075022 Proficient Rx LP BUSPIRONE HYDROCHLORIDE 5 mg/1 90 TABLET in 1 BOTTLE (71205-799-90)
0615-8527-39 0615-8527 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20240918 N/A ANDA ANDA075022 NCS HealthCare of KY, LLC dba Vangard Labs BUSPIRONE HYDROCHLORIDE 30 mg/1 30 TABLET in 1 BLISTER PACK (0615-8527-39)
0615-7714-30 0615-7714 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20120423 N/A ANDA ANDA075022 NCS HealthCare of KY, LLC dba Vangard Labs BUSPIRONE HYDROCHLORIDE 5 mg/1 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7714-30) / 5 TABLET in 1 BLISTER PACK
0615-7714-39 0615-7714 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20120423 N/A ANDA ANDA075022 NCS HealthCare of KY, LLC dba Vangard Labs BUSPIRONE HYDROCHLORIDE 5 mg/1 30 TABLET in 1 BLISTER PACK (0615-7714-39)
63187-904-30 63187-904 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20170901 N/A ANDA ANDA075022 Proficient Rx LP BUSPIRONE HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (63187-904-30)
63187-904-60 63187-904 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20170901 N/A ANDA ANDA075022 Proficient Rx LP BUSPIRONE HYDROCHLORIDE 10 mg/1 60 TABLET in 1 BOTTLE (63187-904-60)
63187-904-90 63187-904 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride Buspirone Hydrochloride TABLET ORAL 20170901 N/A ANDA ANDA075022 Proficient Rx LP BUSPIRONE HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (63187-904-90)
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