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
72789-338-90 72789-338 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230728 N/A ANDA ANDA208706 PD-Rx Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)
80425-0146-1 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 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-1)
80425-0146-2 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 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0146-2)
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)
27241-097-05 27241-097 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20211018 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-05)
27241-097-06 27241-097 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-06)
27241-097-10 27241-097 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-10)
27241-097-90 27241-097 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20211018 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-097-90)
68001-595-04 68001-595 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240222 N/A ANDA ANDA208706 BluePoint Laboratories DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-595-04)
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)
68001-595-08 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)
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)
27241-099-03 27241-099 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-03)
27241-099-40 27241-099 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20211018 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-40)
27241-099-90 27241-099 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-90)
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)
51655-237-25 51655-237 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210423 N/A ANDA ANDA208706 Northwind Health Company, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-237-25)
27241-098-03 27241-098 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-03)
27241-098-09 27241-098 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Ajanta Pharma USA Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-09)
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