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=ANDA078888"
符合检索条件的记录共 70 条，共 4 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
68382-183-05 68382-183 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 30 mg/1 500 TABLET in 1 BOTTLE (68382-183-05)
68382-183-10 68382-183 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 30 mg/1 1000 TABLET in 1 BOTTLE (68382-183-10)
68382-183-14 68382-183 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 30 mg/1 60 TABLET in 1 BOTTLE (68382-183-14)
68382-183-77 68382-183 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 30 mg/1 100 BLISTER PACK in 1 CARTON (68382-183-77) / 1 TABLET in 1 BLISTER PACK (68382-183-30)
68382-180-05 68382-180 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 5 mg/1 500 TABLET in 1 BOTTLE (68382-180-05)
68382-623-01 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 TABLET in 1 BOTTLE (68382-623-01)
68382-623-05 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 500 TABLET in 1 BOTTLE (68382-623-05)
68382-623-10 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 1000 TABLET in 1 BOTTLE (68382-623-10)
68382-623-30 68382-623 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20230321 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 BLISTER PACK in 1 CARTON (68382-623-30) / 10 TABLET in 1 BLISTER PACK
68382-180-10 68382-180 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 5 mg/1 1000 TABLET in 1 BOTTLE (68382-180-10)
68382-180-77 68382-180 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Zydus Pharmaceuticals USA Inc. BUSPIRONE HYDROCHLORIDE 5 mg/1 100 BLISTER PACK in 1 CARTON (68382-180-77) / 1 TABLET in 1 BLISTER PACK (68382-180-30)
0904-6899-61 0904-6899 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20140503 N/A ANDA ANDA078888 Major Pharmaceuticals BUSPIRONE HYDROCHLORIDE 15 mg/1 100 BLISTER PACK in 1 CARTON (0904-6899-61) / 1 TABLET in 1 BLISTER PACK
72162-2199-1 72162-2199 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20231215 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 TABLET in 1 BOTTLE (72162-2199-1)
71335-2820-1 71335-2820 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20251110 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 7.5 mg/1 100 TABLET in 1 BOTTLE (71335-2820-1)
71335-0222-2 71335-0222 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20190411 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 10 mg/1 60 TABLET in 1 BOTTLE (71335-0222-2)
71335-0222-5 71335-0222 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 10 mg/1 180 TABLET in 1 BOTTLE (71335-0222-5)
71335-0222-6 71335-0222 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 10 mg/1 120 TABLET in 1 BOTTLE (71335-0222-6)
70518-0380-0 70518-0380 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20170403 N/A ANDA ANDA078888 REMEDYREPACK INC. BUSPIRONE HYDROCHLORIDE 15 mg/1 30 TABLET in 1 BLISTER PACK (70518-0380-0)
71335-0222-3 71335-0222 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (71335-0222-3)
71335-0222-4 71335-0222 HUMAN PRESCRIPTION DRUG Buspirone hydrochloride Buspirone hydrochloride TABLET ORAL 20211227 N/A ANDA ANDA078888 Bryant Ranch Prepack BUSPIRONE HYDROCHLORIDE 10 mg/1 45 TABLET in 1 BOTTLE (71335-0222-4)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase