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
70518-1139-4 70518-1139 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251227 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-4)
50090-6899-0 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 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6899-0)
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)
70518-1054-0 70518-1054 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180309 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1054-0)
71205-005-30 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-30)
71205-005-60 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-60)
71205-005-90 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-90)
50090-6900-0 50090-6900 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 (50090-6900-0)
68001-594-06 68001-594 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231111 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-594-06)
80425-0311-1 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-1)
80425-0311-2 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-2)
80425-0311-3 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-3)
68001-596-04 68001-596 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230728 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-596-04)
68001-596-08 68001-596 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230728 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-596-08)
71610-403-53 71610-403 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251114 N/A ANDA ANDA208706 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-403-53)
71335-2017-1 71335-2017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220210 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1)
71335-2017-2 71335-2017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220210 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2)
71335-2017-3 71335-2017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220210 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3)
71335-2017-4 71335-2017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220210 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4)
71335-2017-5 71335-2017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220210 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5)
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