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=ANDA203125"
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
0143-9753-25 0143-9753 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20220926 N/A ANDA ANDA203125 Hikma Pharmaceuticals USA Inc. METHYLPREDNISOLONE SODIUM SUCCINATE 40 mg/1 25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9753-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
0143-9754-25 0143-9754 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20220926 N/A ANDA ANDA203125 Hikma Pharmaceuticals USA Inc. METHYLPREDNISOLONE SODIUM SUCCINATE 125 mg/1 25 VIAL, SINGLE-DOSE in 1 CARTON (0143-9754-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (0143-9754-01)
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