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=ANDA076796"
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
71610-636-53 71610-636 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20220224 N/A ANDA ANDA076796 Aphena Pharma Solutions - Tennessee, LLC FUROSEMIDE 80 mg/1 60 TABLET in 1 BOTTLE (71610-636-53)
71610-636-60 71610-636 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20220224 N/A ANDA ANDA076796 Aphena Pharma Solutions - Tennessee, LLC FUROSEMIDE 80 mg/1 90 TABLET in 1 BOTTLE (71610-636-60)
71610-636-80 71610-636 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20220224 N/A ANDA ANDA076796 Aphena Pharma Solutions - Tennessee, LLC FUROSEMIDE 80 mg/1 180 TABLET in 1 BOTTLE (71610-636-80)
72789-030-30 72789-030 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20191205 N/A ANDA ANDA076796 PD-Rx Pharmaceuticals, Inc. FUROSEMIDE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (72789-030-30)
72789-030-60 72789-030 HUMAN PRESCRIPTION DRUG Furosemide furosemide TABLET ORAL 20191205 N/A ANDA ANDA076796 PD-Rx Pharmaceuticals, Inc. FUROSEMIDE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (72789-030-60)
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