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"
符合检索条件的记录共 107 条，共 6 页，当前第 2 页 ，可点击列名称排序
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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
80425-0146-3 80425-0146 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20230614 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-3)
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)
71205-358-30 71205-358 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20191114 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-30)
71205-358-60 71205-358 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20191114 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-60)
71205-358-90 71205-358 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20191114 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-90)
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)
68071-3519-3 68071-3519 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231010 N/A ANDA ANDA208706 NuCare Pharmaceuticals,Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3519-3)
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)
71610-403-60 71610-403 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200309 N/A ANDA ANDA208706 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-403-60)
68788-7672-3 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-3)
68788-7672-6 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-6)
68788-7672-8 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-8)
68788-7672-9 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-9)
51655-237-25 51655-237 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210423 N/A ANDA ANDA208706 Northwind Pharmaceuticals DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)
68788-7672-0 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-0)
68788-7672-1 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-1)
68788-7672-2 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-2)
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