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=ANDA090776"
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
0228-2891-03 0228-2891 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Actavis Pharma, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2891-03)
0228-2891-50 0228-2891 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20140905 N/A ANDA ANDA090776 Actavis Pharma, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2891-50)
76420-236-30 76420-236 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20220707 N/A ANDA ANDA090776 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-30)
76420-236-60 76420-236 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20220707 N/A ANDA ANDA090776 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-60)
76420-236-90 76420-236 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20220707 N/A ANDA ANDA090776 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (76420-236-90)
71205-525-30 71205-525 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20210122 N/A ANDA ANDA090776 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30)
71205-525-60 71205-525 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20210122 N/A ANDA ANDA090776 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60)
71205-525-90 71205-525 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20210122 N/A ANDA ANDA090776 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90)
68071-3779-3 68071-3779 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20250206 N/A ANDA ANDA090776 NuCare Pharmaceuticals,Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3779-3)
0228-2890-06 0228-2890 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Actavis Pharma, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2890-06)
80425-0086-1 80425-0086 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (80425-0086-1)
80425-0086-2 80425-0086 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (80425-0086-2)
71335-1445-1 71335-1445 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-1445-1)
72162-1058-3 72162-1058 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20240801 N/A ANDA ANDA090776 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (72162-1058-3)
63629-8748-1 63629-8748 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-8748-1)
68788-4026-3 68788-4026 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20250915 N/A ANDA ANDA090776 Preferred Phamaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4026-3)
68788-4026-6 68788-4026 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20250915 N/A ANDA ANDA090776 Preferred Phamaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4026-6)
68788-4026-9 68788-4026 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20250915 N/A ANDA ANDA090776 Preferred Phamaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-4026-9)
0228-2892-03 0228-2892 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20131217 N/A ANDA ANDA090776 Actavis Pharma, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2892-03)
0228-2892-96 0228-2892 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE PELLETS ORAL 20140905 N/A ANDA ANDA090776 Actavis Pharma, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (0228-2892-96)
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