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
71335-0409-3 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 20 TABLET in 1 BOTTLE (71335-0409-3)
71335-0409-4 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE (71335-0409-4)
71335-0409-5 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (71335-0409-5)
71335-0409-6 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 10 TABLET in 1 BOTTLE (71335-0409-6)
71335-0409-7 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 120 TABLET in 1 BOTTLE (71335-0409-7)
71335-0409-8 71335-0409 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20220209 N/A ANDA ANDA078916 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 50 TABLET in 1 BOTTLE (71335-0409-8)
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)
67296-1383-3 67296-1383 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160129 N/A ANDA ANDA078916 RedPharm Drug, Inc. FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (67296-1383-3)
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)
0615-8559-05 0615-8559 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250114 N/A ANDA ANDA078916 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 40 mg/1 15 TABLET in 1 BLISTER PACK (0615-8559-05)
0615-8559-39 0615-8559 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20250114 N/A ANDA ANDA078916 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 40 mg/1 30 TABLET in 1 BLISTER PACK (0615-8559-39)
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)
71610-399-30 71610-399 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20200623 N/A ANDA ANDA078916 Aphena Pharma Solutions - Tennessee, LLC FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (71610-399-30)
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