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=ANDA090694"
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
68180-295-06 68180-295 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-06)
68180-295-09 68180-295 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-09)
68180-296-03 68180-296 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-03)
68180-296-06 68180-296 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-06)
68180-296-09 68180-296 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140626 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-09)
68180-297-06 68180-297 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20150715 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-297-06)
68180-295-03 68180-295 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140306 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-03)
68180-294-07 68180-294 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-07)
68180-294-03 68180-294 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090694 Lupin Pharmaceuticals, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-03)
80425-0389-1 80425-0389 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240522 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-1)
80425-0389-2 80425-0389 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240522 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-2)
80425-0389-3 80425-0389 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240522 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-3)
80425-0441-2 80425-0441 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20241022 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-2)
80425-0441-3 80425-0441 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20241022 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-3)
80425-0441-1 80425-0441 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20241022 N/A ANDA ANDA090694 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-1)
0615-8495-05 0615-8495 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240103 N/A ANDA ANDA090694 NCS HealthCare of KY, LLC dba Vangard Labs DULOXETINE HYDROCHLORIDE 30 mg/1 15 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8495-05)
0615-8494-39 0615-8494 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240104 N/A ANDA ANDA090694 NCS HealthCare of KY, LLC dba Vangard Labs DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8494-39)
0615-8496-28 0615-8496 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20241231 N/A ANDA ANDA090694 NCS HealthCare of KY, LLC dba Vangard Labs DULOXETINE HYDROCHLORIDE 60 mg/1 28 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8496-28)
0615-8495-39 0615-8495 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20240103 N/A ANDA ANDA090694 NCS HealthCare of KY, LLC dba Vangard Labs DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8495-39)
0615-8496-39 0615-8496 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine CAPSULE, DELAYED RELEASE ORAL 20231229 N/A ANDA ANDA090694 NCS HealthCare of KY, LLC dba Vangard Labs DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8496-39)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase