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=ANDA211412"
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
69117-0021-1 69117-0021 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 100 mg/1 60 CAPSULE in 1 BOTTLE (69117-0021-1)
69117-0021-2 69117-0021 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 100 mg/1 100 CAPSULE in 1 BOTTLE (69117-0021-2)
69117-0021-3 69117-0021 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (69117-0021-3)
69117-0022-1 69117-0022 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 200 mg/1 60 CAPSULE in 1 BOTTLE (69117-0022-1)
69117-0022-2 69117-0022 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (69117-0022-2)
69117-0022-3 69117-0022 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (69117-0022-3)
69117-0023-1 69117-0023 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 400 mg/1 60 CAPSULE in 1 BOTTLE (69117-0023-1)
69117-0023-2 69117-0023 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 400 mg/1 100 CAPSULE in 1 BOTTLE (69117-0023-2)
69117-0023-3 69117-0023 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 400 mg/1 500 CAPSULE in 1 BOTTLE (69117-0023-3)
69117-0020-3 69117-0020 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 50 mg/1 500 CAPSULE in 1 BOTTLE (69117-0020-3)
69117-0020-2 69117-0020 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 50 mg/1 100 CAPSULE in 1 BOTTLE (69117-0020-2)
69117-0020-1 69117-0020 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20200306 N/A ANDA ANDA211412 Yiling Pharmaceutical, Inc. CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (69117-0020-1)
13668-730-60 13668-730 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (13668-730-60)
13668-732-05 13668-732 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 200 mg/1 500 CAPSULE in 1 BOTTLE (13668-732-05)
13668-733-60 13668-733 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 400 mg/1 60 CAPSULE in 1 BOTTLE (13668-733-60)
13668-731-01 13668-731 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 100 mg/1 100 CAPSULE in 1 BOTTLE (13668-731-01)
13668-731-05 13668-731 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (13668-731-05)
13668-732-01 13668-732 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20240510 N/A ANDA ANDA211412 Torrent Pharmaceuticals Limited CELECOXIB 200 mg/1 100 CAPSULE in 1 BOTTLE (13668-732-01)
81288-020-10 81288-020 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220718 N/A ANDA ANDA211412 EMC PHARMA, LLC CELECOXIB 50 mg/1 60 CAPSULE in 1 BOTTLE (81288-020-10)
81288-021-30 81288-021 HUMAN PRESCRIPTION DRUG Celecoxib Celecoxib CAPSULE ORAL 20220718 N/A ANDA ANDA211412 EMC PHARMA, LLC CELECOXIB 100 mg/1 500 CAPSULE in 1 BOTTLE (81288-021-30)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase