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=ANDA078302"
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
71335-2768-3 71335-2768 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride buspirone hydrochloride TABLET ORAL 20251003 N/A ANDA ANDA078302 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 30 mg/1 56 TABLET in 1 BOTTLE (71335-2768-3)
71335-2768-4 71335-2768 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride buspirone hydrochloride TABLET ORAL 20251003 N/A ANDA ANDA078302 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 30 mg/1 90 TABLET in 1 BOTTLE (71335-2768-4)
71335-2768-5 71335-2768 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride buspirone hydrochloride TABLET ORAL 20251003 N/A ANDA ANDA078302 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 30 mg/1 180 TABLET in 1 BOTTLE (71335-2768-5)
71335-2768-6 71335-2768 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride buspirone hydrochloride TABLET ORAL 20251003 N/A ANDA ANDA078302 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 30 mg/1 15 TABLET in 1 BOTTLE (71335-2768-6)
71335-2768-7 71335-2768 HUMAN PRESCRIPTION DRUG Buspirone Hydrochloride buspirone hydrochloride TABLET ORAL 20251003 N/A ANDA ANDA078302 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 30 mg/1 120 TABLET in 1 BOTTLE (71335-2768-7)
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