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=ANDA219116"
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
67184-0593-2 67184-0593 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION INTRAMUSCULAR; INTRAVENOUS 20240919 N/A ANDA ANDA219116 Qilu Pharmaceutical Co., Ltd. BUMETANIDE .25 mg/mL 10 VIAL in 1 CARTON (67184-0593-2) / 4 mL in 1 VIAL (67184-0593-1)
67184-0594-2 67184-0594 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION INTRAMUSCULAR; INTRAVENOUS 20240919 N/A ANDA ANDA219116 Qilu Pharmaceutical Co., Ltd. BUMETANIDE .25 mg/mL 10 VIAL in 1 CARTON (67184-0594-2) / 10 mL in 1 VIAL (67184-0594-1)
83301-0080-2 83301-0080 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION INTRAMUSCULAR; INTRAVENOUS 20250404 N/A ANDA ANDA219116 Mullan Pharmaceutical Inc. BUMETANIDE .25 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (83301-0080-2) / 4 mL in 1 VIAL, SINGLE-DOSE (83301-0080-1)
83301-0081-2 83301-0081 HUMAN PRESCRIPTION DRUG Bumetanide Bumetanide INJECTION INTRAMUSCULAR; INTRAVENOUS 20250404 N/A ANDA ANDA219116 Mullan Pharmaceutical Inc. BUMETANIDE .25 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (83301-0081-2) / 10 mL in 1 VIAL, MULTI-DOSE (83301-0081-1)
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