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=ANDA202882"
符合检索条件的记录共 97 条，共 5 页，当前第 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
68788-8644-3 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-3)
68788-8644-6 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 CARTON (68788-8644-6)
68788-8644-8 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-8)
68788-8644-9 68788-8644 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240501 N/A ANDA ANDA202882 Preferred Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8644-9)
68071-4864-9 68071-4864 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20190424 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4864-9)
71610-653-53 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-53)
71610-653-60 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-60)
71610-653-80 71610-653 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220714 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-653-80)
76420-668-10 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-10)
76420-669-10 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-10)
76420-669-30 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-30)
76420-669-60 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-60)
76420-669-90 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-90)
76420-671-01 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-01)
76420-671-10 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-10)
76420-671-30 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-30)
76420-671-60 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-60)
76420-671-90 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-90)
76420-668-30 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-30)
76420-668-60 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase