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=ANDA074441"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
25021-321-04 25021-321 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20240601 N/A ANDA ANDA074441 Sagent Pharmaceuticals BUMETANIDE .25 mg/mL 10 VIAL in 1 CARTON (25021-321-04) / 4 mL in 1 VIAL
25021-321-10 25021-321 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20240601 N/A ANDA ANDA074441 Sagent Pharmaceuticals BUMETANIDE .25 mg/mL 10 VIAL in 1 CARTON (25021-321-10) / 10 mL in 1 VIAL
70860-405-04 70860-405 HUMAN PRESCRIPTION DRUG Bumetanide bumetanide INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20220208 20260131 ANDA ANDA074441 Athenex Pharmaceutical Division, LLC. BUMETANIDE .25 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (70860-405-04) / 4 mL in 1 VIAL, SINGLE-DOSE
70860-406-10 70860-406 HUMAN PRESCRIPTION DRUG Bumetanide bumetanide INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS 20220208 20260131 ANDA ANDA074441 Athenex Pharmaceutical Division, LLC. BUMETANIDE .25 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (70860-406-10) / 10 mL in 1 VIAL, MULTI-DOSE
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