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 135 条，共 7 页，当前第 4 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
72189-661-30 72189-661 HUMAN PRESCRIPTION DRUG Duloxetine D/R Duloxetine D/R CAPSULE, DELAYED RELEASE ORAL 20260209 N/A ANDA ANDA208706 Direct_Rx DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-30)
72189-661-60 72189-661 HUMAN PRESCRIPTION DRUG Duloxetine D/R Duloxetine D/R CAPSULE, DELAYED RELEASE ORAL 20260209 N/A ANDA ANDA208706 Direct_Rx DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-60)
71205-602-30 71205-602 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210820 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30)
71205-602-60 71205-602 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210820 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60)
71205-602-90 71205-602 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210820 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)
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)
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)
68788-7672-0 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)
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)
68788-7935-3 68788-7935 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210615 N/A ANDA ANDA208706 Preferred Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-3)
68788-7935-6 68788-7935 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210615 N/A ANDA ANDA208706 Preferred Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-6)
68788-7935-9 68788-7935 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210615 N/A ANDA ANDA208706 Preferred Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7935-9)
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)
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