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=ANDA214785"
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
36000-308-10 36000-308 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20210129 N/A ANDA ANDA214785 Baxter Healthcare Corporation NALOXONE HYDROCHLORIDE .4 mg/mL 10 VIAL, SINGLE-DOSE in 1 CARTON (36000-308-10) / 1 mL in 1 VIAL, SINGLE-DOSE (36000-308-01)
71872-7297-1 71872-7297 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20221116 N/A ANDA ANDA214785 Medical Purchasing Solutions, LLC NALOXONE HYDROCHLORIDE .4 mg/mL 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7297-1) / 1 mL in 1 VIAL, SINGLE-DOSE
43066-142-10 43066-142 HUMAN PRESCRIPTION DRUG naloxone hydrochloride naloxone hydrochloride INJECTION, SOLUTION INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS 20250603 N/A ANDA ANDA214785 Baxter Healthcare Corporation NALOXONE HYDROCHLORIDE 1 mg/mL 10 CARTON in 1 CARTON (43066-142-10) / 1 SYRINGE, GLASS in 1 CARTON (43066-142-01) / 2 mL in 1 SYRINGE, GLASS
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