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=ANDA208521"
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
72266-247-01 72266-247 HUMAN PRESCRIPTION DRUG Sodium Phenylacetate and Sodium Benzoate Sodium Phenylacetate and Sodium Benzoate INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20220818 N/A ANDA ANDA208521 FOSUN PHARMA USA INC SODIUM BENZOATE; SODIUM PHENYLACETATE 100 mg/mL; 100 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-247-01) / 50 mL in 1 VIAL, SINGLE-DOSE
70511-101-50 70511-101 HUMAN PRESCRIPTION DRUG SODIUM PHENYLACETATE AND SODIUM BENZOATE sodium phenylacetate and sodium benzoate INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20170522 N/A ANDA ANDA208521 MAIA PHARMACEUTICALS, INC SODIUM BENZOATE; SODIUM PHENYLACETATE 100 mg/mL; 100 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (70511-101-50) / 50 mL in 1 VIAL, SINGLE-DOSE
67457-844-50 67457-844 HUMAN PRESCRIPTION DRUG Sodium Phenylacetate and Sodium Benzoate Sodium Phenylacetate and Sodium Benzoate INJECTION, SOLUTION, CONCENTRATE INTRAVENOUS 20170523 20240831 ANDA ANDA208521 Mylan Institutional LLC SODIUM BENZOATE; SODIUM PHENYLACETATE 100 mg/mL; 100 mg/mL 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-844-50) / 50 mL in 1 VIAL, SINGLE-DOSE
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