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
68788-7672-2 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-2)
68788-7672-3 68788-7672 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20200228 N/A ANDA ANDA208706 Preferred Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7672-3)
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)
72189-661-30 72189-661 HUMAN PRESCRIPTION DRUG Duloxetine D/R Duloxetine D/R CAPSULE, DELAYED RELEASE ORAL 20260209 N/A ANDA ANDA208706 Direct_Rx DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-30)
72189-661-60 72189-661 HUMAN PRESCRIPTION DRUG Duloxetine D/R Duloxetine D/R CAPSULE, DELAYED RELEASE ORAL 20260209 N/A ANDA ANDA208706 Direct_Rx DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-661-60)
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)
82009-171-10 82009-171 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20250701 N/A ANDA ANDA208706 Quallent Pharmaceuticals Health LLC DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-171-10)
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)
80425-0311-1 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-1)
80425-0311-2 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-2)
80425-0311-3 80425-0311 HUMAN PRESCRIPTION DRUG Duloxetine DR Duloxetine CAPSULE, DELAYED RELEASE ORAL 20230407 N/A ANDA ANDA208706 Advanced Rx Pharmacy of Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-3)
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)
87448-2201-6 87448-2201 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20170316 N/A ANDA ANDA208706 Northwestern Memorial HealthCare DULOXETINE HYDROCHLORIDE 20 mg/1 1 CAPSULE, DELAYED RELEASE in 1 POUCH (87448-2201-6)
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)
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