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
71335-0402-3 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180411 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-3)
76420-636-30 76420-636 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-30)
76420-636-90 76420-636 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA208706 Asclemed USA, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-636-90)
70518-1011-0 70518-1011 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180212 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1011-0)
70518-1011-1 70518-1011 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20190417 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-1)
70518-1011-2 70518-1011 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200504 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-2)
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)
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)
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)
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)
27241-098-10 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 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-098-10)
50090-6900-0 50090-6900 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231211 N/A ANDA ANDA208706 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6900-0)
55700-605-30 55700-605 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180420 20260531 ANDA ANDA208706 Quality Care Products LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-30)
55700-605-60 55700-605 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180420 20260531 ANDA ANDA208706 Quality Care Products LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55700-605-60)
71335-0402-4 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20181030 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-4)
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