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=ANDA202691"
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
0143-9182-01 0143-9182 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20240115 N/A ANDA ANDA202691 Hikma Pharmaceuticals USA Inc. METHYLPREDNISOLONE SODIUM SUCCINATE 1 g/1 1 VIAL, MULTI-DOSE in 1 CARTON (0143-9182-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE
0143-9850-01 0143-9850 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20160101 N/A ANDA ANDA202691 Hikma Pharmaceuticals USA Inc. METHYLPREDNISOLONE SODIUM SUCCINATE 500 mg/1 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9850-01)
0143-9851-01 0143-9851 HUMAN PRESCRIPTION DRUG Methylprednisolone Sodium Succinate Methylprednisolone Sodium Succinate INJECTION, POWDER, FOR SOLUTION INTRAMUSCULAR; INTRAVENOUS 20160101 N/A ANDA ANDA202691 Hikma Pharmaceuticals USA Inc. METHYLPREDNISOLONE SODIUM SUCCINATE 1 g/1 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9851-01)
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