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=ANDA207634"
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
70069-072-10 70069-072 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20170726 N/A ANDA ANDA207634 Somerset Therapeutics, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 10 CARTON in 1 BOX (70069-072-10) / 1 VIAL, GLASS in 1 CARTON (70069-072-01) / 10 mL in 1 VIAL, GLASS
71872-7326-1 71872-7326 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20240619 N/A ANDA ANDA207634 Medical Purchasing Solutions, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 CARTON in 1 BAG (71872-7326-1) / 1 VIAL, GLASS in 1 CARTON / 10 mL in 1 VIAL, GLASS
84549-072-10 84549-072 HUMAN PRESCRIPTION DRUG Naloxone Hydrochloride Naloxone Hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20250919 N/A ANDA ANDA207634 ProPharma Distribution NALOXONE HYDROCHLORIDE .4 mg/mL 10 mL in 1 VIAL, GLASS (84549-072-10)
51662-1426-1 51662-1426 HUMAN PRESCRIPTION DRUG NALOXONE HYDROCHLORIDE NALOXONE HYDROCHLORIDE INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20200110 N/A ANDA ANDA207634 HF Acquisition Co LLC, DBA HealthFirst NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, GLASS in 1 CARTON (51662-1426-1) / 10 mL in 1 VIAL, GLASS
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