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=ANDA075805"
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
71610-470-60 71610-470 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20201009 N/A ANDA ANDA075805 Aphena Pharma Solutions - Tennessee, LLC FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (71610-470-60)
71610-470-80 71610-470 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20201009 N/A ANDA ANDA075805 Aphena Pharma Solutions - Tennessee, LLC FAMOTIDINE 20 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (71610-470-80)
72189-207-90 72189-207 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20210603 N/A ANDA ANDA075805 direct rx FAMOTIDINE 40 mg/1 90 TABLET in 1 BOTTLE (72189-207-90)
72189-207-30 72189-207 HUMAN PRESCRIPTION DRUG FAMOTIDINE FAMOTIDINE TABLET ORAL 20210603 N/A ANDA ANDA075805 direct rx FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE (72189-207-30)
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