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=ANDA078916"
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
82868-077-90 82868-077 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250422 N/A ANDA ANDA078916 Northwind Pharmaceuticals, LLC FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (82868-077-90)
82868-077-60 82868-077 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250723 N/A ANDA ANDA078916 Northwind Pharmaceuticals, LLC FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (82868-077-60)
63187-723-06 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20190901 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 6 TABLET in 1 BOTTLE (63187-723-06)
63187-723-60 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160601 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE (63187-723-60)
63187-723-90 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160601 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE (63187-723-90)
63187-723-00 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160601 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (63187-723-00)
63187-723-10 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20161101 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 10 TABLET in 1 BOTTLE (63187-723-10)
63187-723-30 63187-723 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160601 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (63187-723-30)
62332-001-10 62332-001 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 100 TABLET in 1 CARTON (62332-001-10)
62332-001-91 62332-001 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 1000 TABLET in 1 BOTTLE (62332-001-91)
62332-002-10 62332-002 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 100 TABLET in 1 CARTON (62332-002-10)
62332-002-30 62332-002 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (62332-002-30)
62332-002-31 62332-002 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 100 TABLET in 1 BOTTLE (62332-002-31)
62332-002-71 62332-002 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 500 TABLET in 1 BOTTLE (62332-002-71)
62332-002-91 62332-002 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 40 mg/1 1000 TABLET in 1 BOTTLE (62332-002-91)
62332-001-30 62332-001 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (62332-001-30)
62332-001-31 62332-001 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (62332-001-31)
62332-001-71 62332-001 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Inc. FAMOTIDINE 20 mg/1 500 TABLET in 1 BOTTLE (62332-001-71)
63187-908-30 63187-908 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170901 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (63187-908-30)
63187-908-60 63187-908 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170901 N/A ANDA ANDA078916 Proficient Rx LP FAMOTIDINE 40 mg/1 60 TABLET in 1 BOTTLE (63187-908-60)
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