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=ANDA077634"
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
62756-260-01 62756-260 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 100 mg/1 30 CAPSULE in 1 BOTTLE (62756-260-01)
62756-260-02 62756-260 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 100 mg/1 100 CAPSULE in 1 BOTTLE (62756-260-02)
62756-260-03 62756-260 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 100 mg/1 100 CAPSULE in 1 BOTTLE (62756-260-03)
62756-260-04 62756-260 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 100 mg/1 1000 CAPSULE in 1 BOTTLE (62756-260-04)
62756-258-04 62756-258 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 25 mg/1 1000 CAPSULE in 1 BOTTLE (62756-258-04)
62756-258-01 62756-258 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 25 mg/1 30 CAPSULE in 1 BOTTLE (62756-258-01)
62756-258-02 62756-258 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 25 mg/1 100 CAPSULE in 1 BOTTLE (62756-258-02)
62756-260-05 62756-260 HUMAN PRESCRIPTION DRUG Zonisamide Zonisamide CAPSULE ORAL 20060317 N/A ANDA ANDA077634 Sun Pharmaceutical Industries, Inc. ZONISAMIDE 100 mg/1 500 CAPSULE in 1 BOTTLE (62756-260-05)
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