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 129 条，共 7 页，当前第 5 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
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)
70518-1054-6 70518-1054 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20210609 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1054-6)
70518-1139-0 70518-1139 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180425 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1139-0)
70518-1139-1 70518-1139 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250109 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-1)
70518-1139-2 70518-1139 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250416 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 20 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-2)
70518-1139-3 70518-1139 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250613 N/A ANDA ANDA208706 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1139-3)
71205-005-30 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-30)
71205-005-60 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-60)
71205-005-90 71205-005 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180402 N/A ANDA ANDA208706 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-005-90)
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)
71335-0402-5 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20181112 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-5)
71335-0402-6 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20211227 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-6)
71335-0402-2 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20211227 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-2)
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)
71335-0402-1 71335-0402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20180302 N/A ANDA ANDA208706 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0402-1)
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)
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)
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)
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