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=NDA022020"
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
55154-4232-0 55154-4232 HUMAN PRESCRIPTION DRUG Protonix Delayed-Release pantoprazole sodium GRANULE, DELAYED RELEASE ORAL 20080229 N/A NDA NDA022020 Cardinal Health 107, LLC PANTOPRAZOLE SODIUM 40 mg/1 10 PACKET in 1 BAG (55154-4232-0) / 40 GRANULE, DELAYED RELEASE in 1 PACKET
0008-0844-02 0008-0844 HUMAN PRESCRIPTION DRUG Protonix Delayed-Release PANTOPRAZOLE SODIUM GRANULE, DELAYED RELEASE ORAL 20080229 N/A NDA NDA022020 Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 PACKET in 1 CARTON (0008-0844-02) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (0008-0844-01)
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