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=ANDA208706"
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
27241-164-30 27241-164 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20190325 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-164-30)
50090-6899-1 50090-6899 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231211 N/A ANDA ANDA208706 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6899-1)
55700-605-30 55700-605 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180420 20260531 ANDA ANDA208706 Quality Care Products LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-30)
55700-605-60 55700-605 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180420 20260531 ANDA ANDA208706 Quality Care Products LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-60)
76420-623-01 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-01)
76420-623-20 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250403 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-20)
76420-623-30 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-30)
76420-623-60 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-60)
76420-623-90 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase