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
0615-8558-05 0615-8558 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250116 N/A ANDA ANDA078916 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 20 mg/1 15 TABLET in 1 BLISTER PACK (0615-8558-05)
0615-8558-28 0615-8558 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250116 N/A ANDA ANDA078916 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 20 mg/1 28 TABLET in 1 BLISTER PACK (0615-8558-28)
0615-8558-39 0615-8558 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250116 N/A ANDA ANDA078916 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 20 mg/1 30 TABLET in 1 BLISTER PACK (0615-8558-39)
68071-3201-2 68071-3201 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170324 N/A ANDA ANDA078916 NuCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 20 TABLET in 1 BOTTLE (68071-3201-2)
68071-3201-3 68071-3201 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170324 N/A ANDA ANDA078916 NuCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (68071-3201-3)
68071-3201-6 68071-3201 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170324 N/A ANDA ANDA078916 NuCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE (68071-3201-6)
68071-3201-8 68071-3201 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170324 N/A ANDA ANDA078916 NuCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 180 TABLET in 1 BOTTLE (68071-3201-8)
68071-3201-9 68071-3201 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170324 N/A ANDA ANDA078916 NuCare Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE (68071-3201-9)
46708-294-10 46708-294 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Limited FAMOTIDINE 40 mg/1 100 TABLET in 1 CARTON (46708-294-10)
46708-294-30 46708-294 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 Alembic Pharmaceuticals Limited FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (46708-294-30)
72189-141-60 72189-141 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20201015 N/A ANDA ANDA078916 direct rx FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE (72189-141-60)
72189-141-90 72189-141 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20201015 N/A ANDA ANDA078916 direct rx FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE (72189-141-90)
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)
71335-0231-1 71335-0231 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20180726 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (71335-0231-1)
71335-0231-2 71335-0231 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20180306 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 60 TABLET in 1 BOTTLE (71335-0231-2)
71335-0231-3 71335-0231 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20191111 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 100 TABLET in 1 BOTTLE (71335-0231-3)
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