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=ANDA202038"
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
71335-1165-2 71335-1165 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190321 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1165-2)
50090-5361-0 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)
50090-5361-1 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)
50090-5379-0 50090-5379 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5379-0)
50090-5361-2 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)
60687-725-01 60687-725 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230705 N/A ANDA ANDA202038 American Health Packaging PANTOPRAZOLE SODIUM 20 mg/1 100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)
60760-646-30 60760-646 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220825 N/A ANDA ANDA202038 ST. MARY'S MEDICAL PARK PHARMACY PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30)
68071-4917-3 68071-4917 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20250131 N/A ANDA ANDA202038 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4917-3)
71335-0310-1 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190307 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-1)
71335-0310-2 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190313 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-2)
71335-0310-3 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20190401 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-3)
71335-0310-4 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 58 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-4)
71335-0310-5 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-5)
71335-0310-6 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-6)
71335-0310-7 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-7)
71335-0310-8 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-8)
71335-0310-9 71335-0310 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220502 N/A ANDA ANDA202038 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 40 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0310-9)
35573-428-80 35573-428 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20200420 N/A ANDA ANDA202038 Burel Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 40 mg/1 10 BLISTER PACK in 1 CARTON (35573-428-80) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
51655-797-52 51655-797 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220221 N/A ANDA ANDA202038 Northwind Pharmaceuticals, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-797-52)
67296-1812-7 67296-1812 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 RedPharm Drug PANTOPRAZOLE SODIUM 40 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1812-7)
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