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=ANDA212456"
符合检索条件的记录共 3 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
55150-328-10 55150-328 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191104 N/A ANDA ANDA212456 Eugia US LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, MULTI-DOSE in 1 CARTON (55150-328-10) / 10 mL in 1 VIAL, MULTI-DOSE
55150-328-25 55150-328 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20191104 N/A ANDA ANDA212456 Eugia US LLC NALOXONE HYDROCHLORIDE .4 mg/mL 25 VIAL, MULTI-DOSE in 1 CARTON (55150-328-25) / 10 mL in 1 VIAL, MULTI-DOSE
71872-7215-1 71872-7215 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20200615 N/A ANDA ANDA212456 Medical Purchasing Solutions, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, MULTI-DOSE in 1 BAG (71872-7215-1) / 10 mL in 1 VIAL, MULTI-DOSE
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