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
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)
50090-5940-1 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 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5940-1)
50090-7812-0 50090-7812 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251208 N/A ANDA ANDA208706 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-0)
50090-7812-1 50090-7812 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20251208 N/A ANDA ANDA208706 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-1)
68001-595-05 68001-595 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231110 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-05)
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)
60760-462-60 60760-462 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250916 N/A ANDA ANDA208706 ST. MARY'S MEDICAL PARK PHARMACY DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-462-60)
68001-595-08 68001-595 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230728 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-08)
60760-461-30 60760-461 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20190905 N/A ANDA ANDA208706 ST. MARY'S MEDICAL PARK PHARMACY DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-461-30)
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)
68071-3766-9 68071-3766 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250110 N/A ANDA ANDA208706 NuCare Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)
60760-461-60 60760-461 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20191021 N/A ANDA ANDA208706 ST. MARY'S MEDICAL PARK PHARMACY DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-461-60)
60760-759-30 60760-759 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250715 N/A ANDA ANDA208706 ST. MARY'S MEDICAL PARK PHARMACY DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-759-30)
67046-1451-3 67046-1451 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250207 N/A ANDA ANDA208706 Coupler LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1451-3)
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)
68788-7672-6 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)
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