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
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)
76420-633-00 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250403 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-00)
76420-633-01 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-01)
76420-633-05 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250403 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-05)
76420-633-20 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250403 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-20)
76420-633-30 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-30)
76420-633-60 76420-633 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-60)
76420-623-00 76420-623 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250403 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-00)
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)
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)
50090-5940-0 50090-5940 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20220314 N/A ANDA ANDA208706 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5940-0)
71610-954-30 71610-954 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251014 N/A ANDA ANDA208706 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-30)
71610-954-53 71610-954 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251014 N/A ANDA ANDA208706 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-53)
71610-954-60 71610-954 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251014 N/A ANDA ANDA208706 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-60)
76420-636-01 76420-636 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-01)
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