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=ANDA211824"
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
62332-410-30 62332-410 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 90 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-410-30)
62332-410-91 62332-410 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 90 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-410-91)
62332-411-30 62332-411 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20200615 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 180 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-411-30)
62332-411-91 62332-411 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20200615 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 180 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-411-91)
62332-412-30 62332-412 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 360 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62332-412-30)
62332-412-91 62332-412 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Inc. DEFERASIROX 360 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62332-412-91)
46708-410-30 46708-410 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 90 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-410-30)
46708-410-91 46708-410 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 90 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-410-91)
46708-411-30 46708-411 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20200615 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 180 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-411-30)
46708-411-91 46708-411 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20200615 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 180 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-411-91)
46708-412-30 46708-412 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 360 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (46708-412-30)
46708-412-91 46708-412 HUMAN PRESCRIPTION DRUG DEFERASIROX DEFERASIROX TABLET, FILM COATED ORAL 20191121 N/A ANDA ANDA211824 Alembic Pharmaceuticals Limited DEFERASIROX 360 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (46708-412-91)
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