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=ANDA205014"
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
67457-987-10 67457-987 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191120 N/A ANDA ANDA205014 Mylan Institutional LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (67457-987-10) / 10 mL in 1 VIAL, MULTI-DOSE (67457-987-00)
67457-299-10 67457-299 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20160914 N/A ANDA ANDA205014 Mylan Institutional LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (67457-299-10) / 10 mL in 1 VIAL, MULTI-DOSE (67457-299-00)
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