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=ANDA214201"
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
53041-688-03 53041-688 HUMAN PRESCRIPTION DRUG Diatrizoate Meglumine and Diatrizoate Sodium Diatrizoate Meglumine and Diatrizoate Sodium SOLUTION ORAL; RECTAL 20191218 N/A ANDA ANDA214201 Guardian Drug Company DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM 660 mg/mL; 100 mg/mL 120 mL in 1 BOTTLE, PLASTIC (53041-688-03)
53041-690-03 53041-690 HUMAN PRESCRIPTION DRUG Diatrizoate Meglumine and Diatrizoate Sodium Diatrizoate Meglumine and Diatrizoate Sodium SOLUTION ORAL; RECTAL 20191218 N/A ANDA ANDA214201 Guardian Drug Company DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM 660 mg/mL; 100 mg/mL 120 mL in 1 BOTTLE, GLASS (53041-690-03)
53041-690-09 53041-690 HUMAN PRESCRIPTION DRUG Diatrizoate Meglumine and Diatrizoate Sodium Diatrizoate Meglumine and Diatrizoate Sodium SOLUTION ORAL; RECTAL 20191218 N/A ANDA ANDA214201 Guardian Drug Company DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM 660 mg/mL; 100 mg/mL 30 mL in 1 BOTTLE, GLASS (53041-690-09)
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