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=ANDA090778"
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
71610-401-83 71610-401 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20200226 N/A ANDA ANDA090778 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 3600 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-401-83)
60687-745-01 60687-745 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20230420 20260531 ANDA ANDA090778 American Health Packaging DULOXETINE HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (60687-745-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-745-11)
80425-0014-1 80425-0014 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20221211 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-1)
80425-0014-2 80425-0014 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20221211 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-2)
59651-279-60 59651-279 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-60)
59651-279-78 59651-279 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 20 mg/1 10 BLISTER PACK in 1 CARTON (59651-279-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-279-10)
59651-279-99 59651-279 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-279-99)
60760-951-60 60760-951 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20230724 N/A ANDA ANDA090778 ST. MARY'S MEDICAL PARK PHARMACY DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-951-60)
71610-402-60 71610-402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20200226 N/A ANDA ANDA090778 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)
63187-612-30 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-30)
63187-612-60 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-60)
63187-612-90 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)
59651-280-30 59651-280 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-30)
59651-280-78 59651-280 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 30 mg/1 10 BLISTER PACK in 1 CARTON (59651-280-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (59651-280-10)
59651-280-90 59651-280 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-90)
59651-280-99 59651-280 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Aurobindo Pharma Limited DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (59651-280-99)
63187-666-30 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-30)
63187-666-60 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-60)
63187-666-90 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-90)
60687-723-21 60687-723 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20230425 20260531 ANDA ANDA090778 American Health Packaging DULOXETINE HYDROCHLORIDE 20 mg/1 30 BLISTER PACK in 1 CARTON (60687-723-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase